The document discusses different types of vaccines including whole-organism vaccines using killed or attenuated microbes, purified macromolecules like toxoids and capsular polysaccharides, recombinant vaccines using genes from pathogens, DNA vaccines, and multivalent subunit vaccines. It describes the mechanisms of how vaccines work to stimulate both humoral and cellular immunity, discusses their effectiveness and manufacturing, and associated risks. Recent research areas are also highlighted along with conclusions on the benefits of vaccines.
Vaccines provide immunity to diseases and contain agents that stimulate the immune system. There are several types including whole organism vaccines using killed or attenuated microbes, purified components like toxoids and polysaccharides, recombinant and DNA vaccines. Vaccines work by inducing both antibody and cellular immune responses. While effective, they also carry small risks like adverse reactions that researchers continue working to understand and improve safety.
This document provides information on different types of vaccines including killed, attenuated, toxoid, subunit, and conjugate vaccines. It describes how vaccines work to stimulate the immune system and provide immunity against diseases. The document also discusses vaccine production processes including growing antigens, isolating and purifying them, and adding adjuvants. It provides examples of excipients commonly found in vaccines and concludes by mentioning new vaccines developed in Indonesia to protect fish against various bacterial diseases.
Reverse vaccinology uses genomics and bioinformatics to identify antigens that could be used in vaccines, rather than relying on culturing pathogens. It sequences the genome of a pathogen and predicts potential antigens, allowing development of vaccines for pathogens that cannot be grown in culture. This approach was used to develop a vaccine for Neisseria meningitidis serogroup B, the first reverse vaccinology vaccine approved for use. Traditional vaccinology is limited by only being able to use antigens that are abundant during infection and that the pathogen can be cultured, whereas reverse vaccinology makes all antigens available for vaccine development.
The document discusses the immune system and vaccination. It provides information on:
- The components and functions of the immune system in protecting the body.
- The differences between natural immunity present at birth and acquired immunity developed after exposure to pathogens.
- How the immune system of children is less developed than adults until around age 1.
- The definition of vaccination as administering a substance to prevent disease, typically using a killed or weakened pathogen.
- The early history of vaccination, including Jenner's pioneering use of the cowpox vaccine to prevent smallpox in the late 18th century.
Vaccines provide immunity to diseases by exposing the immune system to agents that resemble disease-causing pathogens. The first vaccine was developed by Edward Jenner in 1796 to prevent smallpox. Since then, vaccines have been created to protect against many additional diseases. Newer vaccines continue to be developed using technologies like recombinant DNA. Vaccines are necessary public health tools that help prevent disease outbreaks in a cost-effective manner.
This document provides an overview of the history and development of vaccine drug delivery systems. It discusses early methods of vaccination including variolation and Edward Jenner's development of the smallpox vaccine in 1796. Major developments include Louis Pasteur's attenuated vaccines in the 1880s, the creation of inactivated toxins in the 1920s, and the polio vaccines of the 1950s. Recent research focuses on new delivery systems like DNA vaccines, viral vectors, and plant vaccines. The document also examines mechanisms of antigen uptake and presentation, types of vaccines, and delivery methods like liposomes, microparticles, and oral vaccination.
This document discusses vaccines and antiviral drugs. It provides details on the history of vaccines including Edward Jenner's pioneering work developing the smallpox vaccine in 1796. It describes the various types of vaccines such as live attenuated vaccines, inactivated vaccines, toxoid vaccines, and conjugate vaccines. The document also discusses the vaccine production process and gives examples of commonly used antiviral drugs for influenza, herpes, and hepatitis.
This document summarizes the history and development of vaccines. It discusses how Edward Jenner developed the smallpox vaccine in 1796 and how vaccines for other diseases like cholera, anthrax, and plague were developed between 1890-1950. Modern vaccines use attenuated or inactivated forms of pathogens. New delivery systems are being researched like DNA vaccines, viral vectors, and plant-based vaccines. Liposomes and virosomes can be used to deliver subunit vaccines and improve immune responses. Oral vaccines are being developed but face challenges with degradation in the gastrointestinal tract.
Vaccines provide immunity to diseases and contain agents that stimulate the immune system. There are several types including whole organism vaccines using killed or attenuated microbes, purified components like toxoids and polysaccharides, recombinant and DNA vaccines. Vaccines work by inducing both antibody and cellular immune responses. While effective, they also carry small risks like adverse reactions that researchers continue working to understand and improve safety.
This document provides information on different types of vaccines including killed, attenuated, toxoid, subunit, and conjugate vaccines. It describes how vaccines work to stimulate the immune system and provide immunity against diseases. The document also discusses vaccine production processes including growing antigens, isolating and purifying them, and adding adjuvants. It provides examples of excipients commonly found in vaccines and concludes by mentioning new vaccines developed in Indonesia to protect fish against various bacterial diseases.
Reverse vaccinology uses genomics and bioinformatics to identify antigens that could be used in vaccines, rather than relying on culturing pathogens. It sequences the genome of a pathogen and predicts potential antigens, allowing development of vaccines for pathogens that cannot be grown in culture. This approach was used to develop a vaccine for Neisseria meningitidis serogroup B, the first reverse vaccinology vaccine approved for use. Traditional vaccinology is limited by only being able to use antigens that are abundant during infection and that the pathogen can be cultured, whereas reverse vaccinology makes all antigens available for vaccine development.
The document discusses the immune system and vaccination. It provides information on:
- The components and functions of the immune system in protecting the body.
- The differences between natural immunity present at birth and acquired immunity developed after exposure to pathogens.
- How the immune system of children is less developed than adults until around age 1.
- The definition of vaccination as administering a substance to prevent disease, typically using a killed or weakened pathogen.
- The early history of vaccination, including Jenner's pioneering use of the cowpox vaccine to prevent smallpox in the late 18th century.
Vaccines provide immunity to diseases by exposing the immune system to agents that resemble disease-causing pathogens. The first vaccine was developed by Edward Jenner in 1796 to prevent smallpox. Since then, vaccines have been created to protect against many additional diseases. Newer vaccines continue to be developed using technologies like recombinant DNA. Vaccines are necessary public health tools that help prevent disease outbreaks in a cost-effective manner.
This document provides an overview of the history and development of vaccine drug delivery systems. It discusses early methods of vaccination including variolation and Edward Jenner's development of the smallpox vaccine in 1796. Major developments include Louis Pasteur's attenuated vaccines in the 1880s, the creation of inactivated toxins in the 1920s, and the polio vaccines of the 1950s. Recent research focuses on new delivery systems like DNA vaccines, viral vectors, and plant vaccines. The document also examines mechanisms of antigen uptake and presentation, types of vaccines, and delivery methods like liposomes, microparticles, and oral vaccination.
This document discusses vaccines and antiviral drugs. It provides details on the history of vaccines including Edward Jenner's pioneering work developing the smallpox vaccine in 1796. It describes the various types of vaccines such as live attenuated vaccines, inactivated vaccines, toxoid vaccines, and conjugate vaccines. The document also discusses the vaccine production process and gives examples of commonly used antiviral drugs for influenza, herpes, and hepatitis.
This document summarizes the history and development of vaccines. It discusses how Edward Jenner developed the smallpox vaccine in 1796 and how vaccines for other diseases like cholera, anthrax, and plague were developed between 1890-1950. Modern vaccines use attenuated or inactivated forms of pathogens. New delivery systems are being researched like DNA vaccines, viral vectors, and plant-based vaccines. Liposomes and virosomes can be used to deliver subunit vaccines and improve immune responses. Oral vaccines are being developed but face challenges with degradation in the gastrointestinal tract.
The document discusses the history and development of vaccines. It begins with early discoveries in the 18th-19th centuries relating to smallpox and rabies vaccines. It then outlines major vaccine discoveries from the 1890s-1990s for diseases such as diphtheria, polio, measles, and hepatitis B. The document also describes different types of traditional and modern vaccines, including how they are prepared and the microorganisms they contain. It provides details on live attenuated, inactivated, subunit, and viral vector vaccines.
This document discusses newer vaccines and an MR vaccination campaign. It provides background on vaccine history and types. Recent developments include vaccines for pneumococcal, influenza, meningococcal, HPV, and rotavirus. Future vaccines discussed include ones for HIV. The document also outlines the need for vaccination, recently added vaccines in India's national program, and details of vaccination schedules and target groups for campaigns like one for MR in 2017.
Vaccines are biological preparations that improve immunity to particular diseases. They work by containing an agent that resembles a disease-causing microorganism, which stimulates the immune system to recognize and destroy it. Vaccination is the most effective method of preventing infectious diseases and has been largely responsible for eradicating smallpox and restricting diseases like polio. There are several types of vaccines including live attenuated, inactivated, subunit, toxoid, conjugate, DNA, and recombinant vector vaccines. Vaccines must undergo clinical trials and require careful storage and transport to maintain effectiveness.
The document provides an overview of the history and development of vaccines. It discusses key events like Jenner's development of the smallpox vaccine in 1796 and the eradication of smallpox. It describes different types of vaccines including live-attenuated, inactivated, toxoid, subunit, conjugate, and DNA vaccines. The mechanisms of how vaccines work and produce immunity are also explained. The document traces the evolution of vaccines from whole organism approaches to modern techniques like recombinant DNA technology.
This is an immunology lecture for medical students. it helps student to understand the importance of immunization in clinical practice. resident doctors can also benefit immensely with this lecture.
Vaccines work by exposing the immune system to antigens from pathogens to induce an immune response. Major types include whole organism vaccines using live attenuated or killed pathogens, as well as purified components like toxoids, polysaccharides, and recombinant antigens. Current COVID-19 vaccines use viral vectors or genetic material to produce antigens and trigger protective immunity. Vaccines have saved millions of lives through immunization programs by conferring protection against viral and bacterial diseases.
This document provides information about vaccines and their history. It discusses that the first successful vaccine was developed by Edward Jenner in 1796 for smallpox. It then outlines the development of several other important vaccines from 1881 to 2020, including vaccines for anthrax, rabies, diphtheria, tetanus, polio, measles, mumps, rubella, hepatitis B, chickenpox, rotavirus, hepatitis A, pneumococcal disease, HPV, Ebola, and COVID-19. The document also describes the main types of vaccines, such as inactivated, attenuated, toxoid, subunit, recombinant, conjugate, and mRNA vaccines.
Vaccines work by introducing a harmless version of a pathogen into the body to stimulate an immune response without causing illness. There are several types of vaccines including live attenuated, killed/inactivated, subunit, toxoid, conjugate, and recombinant vaccines. An ideal vaccine would provide long-lasting immunity after a single dose, stimulate both antibody and cellular immune responses, be safe, stable, and inexpensive to produce.
what is vaccine
History of vaccine
types of vaccines
live attenuated vaccine
inactivated vaccine
taxoid vaccine
reconbinant vaccine
advantages of vaccine
disadvantages of vaccine
vaccine reaction
mechanism of vaccine
antiviral
antiviral mechanism
mechanism of antivirals
Vaccines work by exposing the immune system to antigens from pathogens. This stimulates the body to develop immunity against future infections from those pathogens. Edward Jenner developed the first vaccine for smallpox in 1796 by using cowpox to provide protection against smallpox. There are several types of vaccines including live attenuated, inactivated, subunit, toxoid, conjugate, DNA, and recombinant vector vaccines. Vaccines must go through multiple stages of testing before being approved for public use to ensure they are safe and effective. An ideal vaccine would provide long-lasting immunity after a single dose with a strong safety profile.
This document provides information about different types of vaccines. It discusses inactivated, attenuated, toxoid, subunit, conjugate, dendritic cell, recombinant vector, DNA, synthetic, and live vector vaccines. Key points include:
- Vaccines work by eliciting an immune response to an antigen to produce immunity against a pathogen without causing disease.
- Inactivated vaccines use killed pathogens, while attenuated vaccines use weakened live pathogens. Toxoid vaccines use inactivated toxins.
- Subunit vaccines use fragments of pathogens like viral surface proteins. Conjugate vaccines link polysaccharides to proteins to stimulate immunity.
- Emerging vaccine types include dendritic cell vaccines, recombinant vector vaccines that combine pathogens, DNA
This document discusses various biologics including antigens, antibodies, immunoglobulins, immunity, and different types of vaccines. It provides details on antigens, the 5 major immunoglobulin classes in humans, natural and acquired immunity, and active vs passive immunity. The document also summarizes many common vaccines such as influenza, polio, measles, mumps, hepatitis B, and others, describing what each vaccine is used for, how it works, dosing recommendations, and potential side effects.
1. The document discusses different types of vaccines including live attenuated, inactivated, subunit, toxoid, conjugate, DNA, and recombinant vector vaccines.
2. It describes how saponins can be used as vaccine adjuvants to increase the immune response, with examples like Quil A that stimulate both Th1 response and cytotoxic T-cells.
3. Research into new vaccines is conducted by organizations like WHO and NIAID to develop vaccines for diseases like HIV/AIDS.
This document provides an overview of vaccines, including their history, types, and uses. It discusses how Edward Jenner developed the smallpox vaccine in 1796 and how Louis Pasteur later developed vaccines for chicken cholera and anthrax in the 1880s. The document outlines seven main types of vaccines: live attenuated, inactivated, subunit, toxoid, conjugate, DNA, and recombinant vector vaccines. It also discusses saponins' potential as vaccine adjuvants and research efforts to develop vaccines for diseases like HIV.
This document provides an overview of vaccines, including their history, types, and uses. It discusses how Edward Jenner developed the smallpox vaccine in 1796 and how Louis Pasteur later developed vaccines for chicken cholera and anthrax in the 1880s. The document outlines seven main types of vaccines: live attenuated, inactivated, subunit, toxoid, conjugate, DNA, and recombinant vector vaccines. It also discusses saponins' potential as vaccine adjuvants and research efforts to develop vaccines, such as for HIV.
This document provides an overview of vaccines, including their history, types, and uses. It discusses how Edward Jenner developed the smallpox vaccine in 1796 and how Louis Pasteur later developed vaccines for chicken cholera and anthrax in the 1880s. The document outlines seven main types of vaccines: live attenuated, inactivated, subunit, toxoid, conjugate, DNA, and recombinant vector vaccines. It also discusses saponins' potential as vaccine adjuvants and research efforts by organizations like WHO and NIAID to develop new vaccines.
This document provides an overview of vaccines, including their history, types, and uses. It discusses how Edward Jenner developed the smallpox vaccine in 1796 and how Louis Pasteur later developed vaccines for chicken cholera and anthrax in the 1880s. The document outlines seven main types of vaccines: live attenuated, inactivated, subunit, toxoid, conjugate, DNA, and recombinant vector vaccines. It also discusses saponins' potential as vaccine adjuvants and research efforts to develop vaccines, such as for HIV.
This document provides an overview of vaccines, including their history, types, and uses. It discusses how Edward Jenner developed the smallpox vaccine in 1796 and how Louis Pasteur later developed vaccines for chicken cholera and anthrax in the 1880s. The document outlines seven main types of vaccines: live attenuated, inactivated, subunit, toxoid, conjugate, DNA, and recombinant vector vaccines. It also discusses saponins' potential as vaccine adjuvants and research efforts to develop vaccines, such as for HIV.
Edible vaccines use transgenic plants to produce antigens from pathogens in a form that stimulates both mucosal and systemic immunity when eaten. They are a low-cost oral alternative to traditional vaccines that don't require refrigeration or trained medical professionals for administration. Several plant species have been engineered to produce vaccine antigens for diseases like ETEC, norovirus, cholera, hepatitis B, and measles, with some human trials showing promise. However, more research is still needed to address challenges like immunotolerance and ensuring consistent antigen levels across plants.
The document discusses the history and development of vaccines. It begins with early discoveries in the 18th-19th centuries relating to smallpox and rabies vaccines. It then outlines major vaccine discoveries from the 1890s-1990s for diseases such as diphtheria, polio, measles, and hepatitis B. The document also describes different types of traditional and modern vaccines, including how they are prepared and the microorganisms they contain. It provides details on live attenuated, inactivated, subunit, and viral vector vaccines.
This document discusses newer vaccines and an MR vaccination campaign. It provides background on vaccine history and types. Recent developments include vaccines for pneumococcal, influenza, meningococcal, HPV, and rotavirus. Future vaccines discussed include ones for HIV. The document also outlines the need for vaccination, recently added vaccines in India's national program, and details of vaccination schedules and target groups for campaigns like one for MR in 2017.
Vaccines are biological preparations that improve immunity to particular diseases. They work by containing an agent that resembles a disease-causing microorganism, which stimulates the immune system to recognize and destroy it. Vaccination is the most effective method of preventing infectious diseases and has been largely responsible for eradicating smallpox and restricting diseases like polio. There are several types of vaccines including live attenuated, inactivated, subunit, toxoid, conjugate, DNA, and recombinant vector vaccines. Vaccines must undergo clinical trials and require careful storage and transport to maintain effectiveness.
The document provides an overview of the history and development of vaccines. It discusses key events like Jenner's development of the smallpox vaccine in 1796 and the eradication of smallpox. It describes different types of vaccines including live-attenuated, inactivated, toxoid, subunit, conjugate, and DNA vaccines. The mechanisms of how vaccines work and produce immunity are also explained. The document traces the evolution of vaccines from whole organism approaches to modern techniques like recombinant DNA technology.
This is an immunology lecture for medical students. it helps student to understand the importance of immunization in clinical practice. resident doctors can also benefit immensely with this lecture.
Vaccines work by exposing the immune system to antigens from pathogens to induce an immune response. Major types include whole organism vaccines using live attenuated or killed pathogens, as well as purified components like toxoids, polysaccharides, and recombinant antigens. Current COVID-19 vaccines use viral vectors or genetic material to produce antigens and trigger protective immunity. Vaccines have saved millions of lives through immunization programs by conferring protection against viral and bacterial diseases.
This document provides information about vaccines and their history. It discusses that the first successful vaccine was developed by Edward Jenner in 1796 for smallpox. It then outlines the development of several other important vaccines from 1881 to 2020, including vaccines for anthrax, rabies, diphtheria, tetanus, polio, measles, mumps, rubella, hepatitis B, chickenpox, rotavirus, hepatitis A, pneumococcal disease, HPV, Ebola, and COVID-19. The document also describes the main types of vaccines, such as inactivated, attenuated, toxoid, subunit, recombinant, conjugate, and mRNA vaccines.
Vaccines work by introducing a harmless version of a pathogen into the body to stimulate an immune response without causing illness. There are several types of vaccines including live attenuated, killed/inactivated, subunit, toxoid, conjugate, and recombinant vaccines. An ideal vaccine would provide long-lasting immunity after a single dose, stimulate both antibody and cellular immune responses, be safe, stable, and inexpensive to produce.
what is vaccine
History of vaccine
types of vaccines
live attenuated vaccine
inactivated vaccine
taxoid vaccine
reconbinant vaccine
advantages of vaccine
disadvantages of vaccine
vaccine reaction
mechanism of vaccine
antiviral
antiviral mechanism
mechanism of antivirals
Vaccines work by exposing the immune system to antigens from pathogens. This stimulates the body to develop immunity against future infections from those pathogens. Edward Jenner developed the first vaccine for smallpox in 1796 by using cowpox to provide protection against smallpox. There are several types of vaccines including live attenuated, inactivated, subunit, toxoid, conjugate, DNA, and recombinant vector vaccines. Vaccines must go through multiple stages of testing before being approved for public use to ensure they are safe and effective. An ideal vaccine would provide long-lasting immunity after a single dose with a strong safety profile.
This document provides information about different types of vaccines. It discusses inactivated, attenuated, toxoid, subunit, conjugate, dendritic cell, recombinant vector, DNA, synthetic, and live vector vaccines. Key points include:
- Vaccines work by eliciting an immune response to an antigen to produce immunity against a pathogen without causing disease.
- Inactivated vaccines use killed pathogens, while attenuated vaccines use weakened live pathogens. Toxoid vaccines use inactivated toxins.
- Subunit vaccines use fragments of pathogens like viral surface proteins. Conjugate vaccines link polysaccharides to proteins to stimulate immunity.
- Emerging vaccine types include dendritic cell vaccines, recombinant vector vaccines that combine pathogens, DNA
This document discusses various biologics including antigens, antibodies, immunoglobulins, immunity, and different types of vaccines. It provides details on antigens, the 5 major immunoglobulin classes in humans, natural and acquired immunity, and active vs passive immunity. The document also summarizes many common vaccines such as influenza, polio, measles, mumps, hepatitis B, and others, describing what each vaccine is used for, how it works, dosing recommendations, and potential side effects.
1. The document discusses different types of vaccines including live attenuated, inactivated, subunit, toxoid, conjugate, DNA, and recombinant vector vaccines.
2. It describes how saponins can be used as vaccine adjuvants to increase the immune response, with examples like Quil A that stimulate both Th1 response and cytotoxic T-cells.
3. Research into new vaccines is conducted by organizations like WHO and NIAID to develop vaccines for diseases like HIV/AIDS.
This document provides an overview of vaccines, including their history, types, and uses. It discusses how Edward Jenner developed the smallpox vaccine in 1796 and how Louis Pasteur later developed vaccines for chicken cholera and anthrax in the 1880s. The document outlines seven main types of vaccines: live attenuated, inactivated, subunit, toxoid, conjugate, DNA, and recombinant vector vaccines. It also discusses saponins' potential as vaccine adjuvants and research efforts to develop vaccines for diseases like HIV.
This document provides an overview of vaccines, including their history, types, and uses. It discusses how Edward Jenner developed the smallpox vaccine in 1796 and how Louis Pasteur later developed vaccines for chicken cholera and anthrax in the 1880s. The document outlines seven main types of vaccines: live attenuated, inactivated, subunit, toxoid, conjugate, DNA, and recombinant vector vaccines. It also discusses saponins' potential as vaccine adjuvants and research efforts to develop vaccines, such as for HIV.
This document provides an overview of vaccines, including their history, types, and uses. It discusses how Edward Jenner developed the smallpox vaccine in 1796 and how Louis Pasteur later developed vaccines for chicken cholera and anthrax in the 1880s. The document outlines seven main types of vaccines: live attenuated, inactivated, subunit, toxoid, conjugate, DNA, and recombinant vector vaccines. It also discusses saponins' potential as vaccine adjuvants and research efforts by organizations like WHO and NIAID to develop new vaccines.
This document provides an overview of vaccines, including their history, types, and uses. It discusses how Edward Jenner developed the smallpox vaccine in 1796 and how Louis Pasteur later developed vaccines for chicken cholera and anthrax in the 1880s. The document outlines seven main types of vaccines: live attenuated, inactivated, subunit, toxoid, conjugate, DNA, and recombinant vector vaccines. It also discusses saponins' potential as vaccine adjuvants and research efforts to develop vaccines, such as for HIV.
This document provides an overview of vaccines, including their history, types, and uses. It discusses how Edward Jenner developed the smallpox vaccine in 1796 and how Louis Pasteur later developed vaccines for chicken cholera and anthrax in the 1880s. The document outlines seven main types of vaccines: live attenuated, inactivated, subunit, toxoid, conjugate, DNA, and recombinant vector vaccines. It also discusses saponins' potential as vaccine adjuvants and research efforts to develop vaccines, such as for HIV.
Edible vaccines use transgenic plants to produce antigens from pathogens in a form that stimulates both mucosal and systemic immunity when eaten. They are a low-cost oral alternative to traditional vaccines that don't require refrigeration or trained medical professionals for administration. Several plant species have been engineered to produce vaccine antigens for diseases like ETEC, norovirus, cholera, hepatitis B, and measles, with some human trials showing promise. However, more research is still needed to address challenges like immunotolerance and ensuring consistent antigen levels across plants.
Describing and Interpreting an Immersive Learning Case with the Immersion Cub...Leonel Morgado
Current descriptions of immersive learning cases are often difficult or impossible to compare. This is due to a myriad of different options on what details to include, which aspects are relevant, and on the descriptive approaches employed. Also, these aspects often combine very specific details with more general guidelines or indicate intents and rationales without clarifying their implementation. In this paper we provide a method to describe immersive learning cases that is structured to enable comparisons, yet flexible enough to allow researchers and practitioners to decide which aspects to include. This method leverages a taxonomy that classifies educational aspects at three levels (uses, practices, and strategies) and then utilizes two frameworks, the Immersive Learning Brain and the Immersion Cube, to enable a structured description and interpretation of immersive learning cases. The method is then demonstrated on a published immersive learning case on training for wind turbine maintenance using virtual reality. Applying the method results in a structured artifact, the Immersive Learning Case Sheet, that tags the case with its proximal uses, practices, and strategies, and refines the free text case description to ensure that matching details are included. This contribution is thus a case description method in support of future comparative research of immersive learning cases. We then discuss how the resulting description and interpretation can be leveraged to change immersion learning cases, by enriching them (considering low-effort changes or additions) or innovating (exploring more challenging avenues of transformation). The method holds significant promise to support better-grounded research in immersive learning.
Current Ms word generated power point presentation covers major details about the micronuclei test. It's significance and assays to conduct it. It is used to detect the micronuclei formation inside the cells of nearly every multicellular organism. It's formation takes place during chromosomal sepration at metaphase.
Travis Hills of MN is Making Clean Water Accessible to All Through High Flux ...Travis Hills MN
By harnessing the power of High Flux Vacuum Membrane Distillation, Travis Hills from MN envisions a future where clean and safe drinking water is accessible to all, regardless of geographical location or economic status.
ESA/ACT Science Coffee: Diego Blas - Gravitational wave detection with orbita...Advanced-Concepts-Team
Presentation in the Science Coffee of the Advanced Concepts Team of the European Space Agency on the 07.06.2024.
Speaker: Diego Blas (IFAE/ICREA)
Title: Gravitational wave detection with orbital motion of Moon and artificial
Abstract:
In this talk I will describe some recent ideas to find gravitational waves from supermassive black holes or of primordial origin by studying their secular effect on the orbital motion of the Moon or satellites that are laser ranged.
The cost of acquiring information by natural selectionCarl Bergstrom
This is a short talk that I gave at the Banff International Research Station workshop on Modeling and Theory in Population Biology. The idea is to try to understand how the burden of natural selection relates to the amount of information that selection puts into the genome.
It's based on the first part of this research paper:
The cost of information acquisition by natural selection
Ryan Seamus McGee, Olivia Kosterlitz, Artem Kaznatcheev, Benjamin Kerr, Carl T. Bergstrom
bioRxiv 2022.07.02.498577; doi: https://doi.org/10.1101/2022.07.02.498577
The debris of the ‘last major merger’ is dynamically youngSérgio Sacani
The Milky Way’s (MW) inner stellar halo contains an [Fe/H]-rich component with highly eccentric orbits, often referred to as the
‘last major merger.’ Hypotheses for the origin of this component include Gaia-Sausage/Enceladus (GSE), where the progenitor
collided with the MW proto-disc 8–11 Gyr ago, and the Virgo Radial Merger (VRM), where the progenitor collided with the
MW disc within the last 3 Gyr. These two scenarios make different predictions about observable structure in local phase space,
because the morphology of debris depends on how long it has had to phase mix. The recently identified phase-space folds in Gaia
DR3 have positive caustic velocities, making them fundamentally different than the phase-mixed chevrons found in simulations
at late times. Roughly 20 per cent of the stars in the prograde local stellar halo are associated with the observed caustics. Based
on a simple phase-mixing model, the observed number of caustics are consistent with a merger that occurred 1–2 Gyr ago.
We also compare the observed phase-space distribution to FIRE-2 Latte simulations of GSE-like mergers, using a quantitative
measurement of phase mixing (2D causticality). The observed local phase-space distribution best matches the simulated data
1–2 Gyr after collision, and certainly not later than 3 Gyr. This is further evidence that the progenitor of the ‘last major merger’
did not collide with the MW proto-disc at early times, as is thought for the GSE, but instead collided with the MW disc within
the last few Gyr, consistent with the body of work surrounding the VRM.
Sexuality - Issues, Attitude and Behaviour - Applied Social Psychology - Psyc...PsychoTech Services
A proprietary approach developed by bringing together the best of learning theories from Psychology, design principles from the world of visualization, and pedagogical methods from over a decade of training experience, that enables you to: Learn better, faster!
Mending Clothing to Support Sustainable Fashion_CIMaR 2024.pdfSelcen Ozturkcan
Ozturkcan, S., Berndt, A., & Angelakis, A. (2024). Mending clothing to support sustainable fashion. Presented at the 31st Annual Conference by the Consortium for International Marketing Research (CIMaR), 10-13 Jun 2024, University of Gävle, Sweden.
ESR spectroscopy in liquid food and beverages.pptxPRIYANKA PATEL
With increasing population, people need to rely on packaged food stuffs. Packaging of food materials requires the preservation of food. There are various methods for the treatment of food to preserve them and irradiation treatment of food is one of them. It is the most common and the most harmless method for the food preservation as it does not alter the necessary micronutrients of food materials. Although irradiated food doesn’t cause any harm to the human health but still the quality assessment of food is required to provide consumers with necessary information about the food. ESR spectroscopy is the most sophisticated way to investigate the quality of the food and the free radicals induced during the processing of the food. ESR spin trapping technique is useful for the detection of highly unstable radicals in the food. The antioxidant capability of liquid food and beverages in mainly performed by spin trapping technique.
Authoring a personal GPT for your research and practice: How we created the Q...Leonel Morgado
Thematic analysis in qualitative research is a time-consuming and systematic task, typically done using teams. Team members must ground their activities on common understandings of the major concepts underlying the thematic analysis, and define criteria for its development. However, conceptual misunderstandings, equivocations, and lack of adherence to criteria are challenges to the quality and speed of this process. Given the distributed and uncertain nature of this process, we wondered if the tasks in thematic analysis could be supported by readily available artificial intelligence chatbots. Our early efforts point to potential benefits: not just saving time in the coding process but better adherence to criteria and grounding, by increasing triangulation between humans and artificial intelligence. This tutorial will provide a description and demonstration of the process we followed, as two academic researchers, to develop a custom ChatGPT to assist with qualitative coding in the thematic data analysis process of immersive learning accounts in a survey of the academic literature: QUAL-E Immersive Learning Thematic Analysis Helper. In the hands-on time, participants will try out QUAL-E and develop their ideas for their own qualitative coding ChatGPT. Participants that have the paid ChatGPT Plus subscription can create a draft of their assistants. The organizers will provide course materials and slide deck that participants will be able to utilize to continue development of their custom GPT. The paid subscription to ChatGPT Plus is not required to participate in this workshop, just for trying out personal GPTs during it.
4. •British physician Edward Jenner, who in 1796 used the cowpox virus (Latin variola
vaccinia) to confer protectionagainst smallpox.
•In 1885 the French microbiologist Louis Pasteur and Emile Roux developed the
first vaccine against rabies.
Introduction
A vaccine is a biological preparation that improves immunity to a particular disease. It
contains certain agents that not only resembles a disease-causing microorganism but it also
stimulates body’s immune sustem recognize the foreign agents.
History:
Definition:
(Ref: www.wikipedia.org, www.britannica.com, www.pathmicro.med.sc.edu)
4
5. 5
Vaccines are dead or inactivated organisms or purified products derived from
them. There are several types of vaccines in use. They are:
Types
• Whole-Organism Vaccines
➢Killed
➢Attenuated
• Purified Macromoleculesas Vaccines
➢Toxoids
➢Capsular polysaccharides
➢Recombinant microbial antigens/Surface antigens
• Recombinant vaccine
• DNA vaccine
• Multivalent Subunit Vaccines (Ref: Kuby, book for Immunology)
6. 6
Many of the common vaccines currently in use consist of inactivated (killed) or live but
attenuated (avirulent) bacterial cells or viral particles.
Whole-OrganismVaccines
➢ Killed/Inactivated.
➢ Attenuated.
Killed/ Inactivated: Some vaccines contain killed, but previously virulent, micro-
organisms that have been destroyed with chemicals, heat, radioactivity or antibiotics.
Attenuated: Some vaccines contain live, attenuated microorganisms. Many of these are
live viruses that have been cultivated under conditions that disable their virulent
properties, or which use closely related but less dangerous organisms to produce a broad
immune response.
(Ref: Kuby, book for Immunology)
7. • BCG by growing TB in high cocentrations of bile.
• Treating Salmonella typhi with nitrosoguanidine, a
mutant strain lacking some enzymes that are
responsible for the virulence was isolated
• Th has been done with a herpesvirus vaccine for pigs,
in which the thymidine kinase gene was removed.
Because thymidine kinase is required for the virus to
grow in certain types of cells (e.g., neurons), removal of
this gene renderedthe virus incapable of causing
disease.
• A live, attenuated vaccine against infl uenza was
developed recently under the name FluMist. The virus
was grown at lower-than-normal temperaturesuntil a
coldadapted strain resulted that is unable to grow at
human body temperatureof 37ºC.
7
8. 8
Disease or pathogen Type of vaccine
WHOLE ORGANISMS
Bacterial cells
Anthrax
Cholera
Pertussis*
Plague
Tuberculosis
Typhoid
Inactivated
Inactivated
Inactivated
Inactivated
Live attenuated
Live attenuated
Classificationof commonvaccinesfor humans:
(Ref: Kuby, book for Immunology)
9. 9
Disease or pathogen Type of vaccine
Viral particles
Hepatitis A
Influenza
Measles
Polio (Sabin)
Polio (Salk)
Rabies
Rotavirus
Varicella zoster (chickenpox)
Yellow fever
Inactivated
Inactivated
Live attenuated
Live attenuated
Inactivated
Inactivated
Live attenuated
Live attenuated
Live attenuated
(Ref: Kuby, book for Immunology)
13. 13
Inactivatedexotoxins/Toxoid
• Toxoids are vaccines which consist of exotoxins that have been inactivated,
either by heat or chemicals. These vaccines are intended to build immunity
against the toxins, but not necessarily the bacteria that produce the toxins.
• Some examples are botulinumantitoxin and diphtheria antitoxin.
Fig: Modificationof toxin to toxoid
(Ref: Kuby, www2a.cdc.gov)
14. 14
• The virulence of some pathogenic bacteria depends primarily on the anti
phagocytic propertiesof their hydrophilic polysaccharide capsule.
• Coating of the capsule with antibodies and or complement greatly increases
the ability of macrophages and neutrophilsto phagocytose such pathogens.
• The current vaccine for Streptococcus pneumoniae, which causes
pneumococcal pneumonia, consists of 23 antigenically different capsular
polysaccharides.
Capsularpolysaccharides
(Ref: Kuby, www2a.cdc.gov)
15. 15
• The gene encoding any immunogenic protein can be cloned and expressed
in bacterial, yeast, or mammalian cells using recombinant DNA technology.
• The first such recombinant antigen vaccine approved for human use is the
hepatitis B vaccine. This vaccine was developed by cloning the gene for the
major surface antigen of hepatitis B virus (HBsAg) and expressing it in yeast
cells.
Recombinantmicrobialantigens/Surfaceantigen
(Ref: Kuby, bookfor Immunology)
17. Conjugate vaccines
• H aemophilus i nfl uenzae type b (Hib): type b capsular polysaccharide
covalently linked to a protein carrier, tetanus toxoid.
• capsular Neisseria polysaccharide antigens joined to the highly
immunogenic diphtheria toxoid protein.
17
19. .
• vaccinia virus,
• the canarypox virus,
• attenuated poliovirus, adenoviruses,
• Attenuated strains of Salmonella ,
• the BCG strain of Mycobacterium
bovis ,
• and certain strains of Streptococcus that normally
exist in the oral cavity
19
22. • No refrigeration
• cheap
• Both humoral and cell mediated immunity
• Ease of delivery (gold coated DNA)
• Prolonged expression of the antigen, enhancing the induction
of immunological memory.
• In addition, the same plasmid vector can be customtailored
to insert DNA encoding a variety of proteins, which allows the
simultaneous manufacture of a variety of DNA vaccines for
different pathogens, saving time and money.
22
27. 27
(Ref: Kuby, bookfor Immunology
Detergentto proteinantigens
Fig: b. Detergent extracted membrane antigens or antigenic peptides
c. ISCOM delivery of antigen into cell
29. 29
Vaccines do not guarantee completeprotection from a disease.
Adjuvants:
•An adjuvant (Latin, adiuvare: to aid) is a pharmacological or immunological
agent that modifies the effect of other agents, such as a drug or vaccine. They
are often included in vaccines to enhance the recipient's immune response to a
supplied antigen, while keeping the injected foreign material to a minimum.
Effectiveness
(Ref: www.wikipedia.org)
30. 30
• The primary risk associated with vaccines, especially vaccines that utilize live
organisms, is that the vaccine itself causes illness.
•Another risk is that the vaccine may behave as a super antigen and over stimulate the
immune system.
•Yet a third risk is that some individuals may have an allergic reaction to the vaccine,
especially vaccines produced in Embryonated chicken eggs and in transgenic plants.
Risksassociatedwithvaccines
Vaccines also have some sort of risks, like:
(Ref: www.wikipedia.org)
31. 31
• Approaches for designing a preventive HIV vaccine.
• Vaccine against Dengue Vaccine.
• NIH Scientists Identify New HIV-Inhibiting Protein.
•NIH Scientists Find Cause of Rare Immune Disease: Genetic Mutation Leads to Cold
Allergy, Immune Deficiency and Autoimmunity.
• NIH Found a Gene That May Play a Role in Type 1 Diabetes.
RecentResearch:
(Ref: www.niaid.nih.gov)
32. 32
Vaccines are one of the most effective health interventions
ever developed. Three types of vaccines are currently used in humans: attenuated
(avirulent) microorganisms, inactivated (killed) microorganisms, or purified
macromolecules. Recombinant vector vaccine and Plasmid DNA vaccines are also used.
They induce both humoral and cell-mediated immunity. Some boosters (called adjuvants)
are also used in association with vaccines for increasing the immune response. As the
vaccines have a lot of benefits, they do carry some harmful effects too.
Conclusion