This document summarizes the components of the innate immune system. It discusses three lines of defense: mechanical barriers like skin and mucus; chemical inhibitors like enzymes and pH levels; and normal flora bacteria. The second line of defense includes natural killer cells and phagocytes like neutrophils and macrophages that ingest and destroy microbes. Soluble factors in the blood also help, like acute phase proteins, complement proteins, and interferons. Phagocytosis is described as the process of chemotaxis, attachment, ingestion, and killing of microbes inside phagocytes. Tissue damage can trigger an inflammatory response with the release of chemical mediators that cause redness, heat, and swelling to isolate and destroy invading pathogens.
Functional Genomics of Plant Pathogen interactions in Wheat Rust PathosystemSenthil Natesan
Cereal rust fungi are pathogens of major importance to agriculture, threatening cereal production worldwide. Targeted breeding for resistance, based on information from fungal surveys and population structure analyses of virulence, has been effective. Nevertheless, breakdown of resistance occurs frequently and continued efforts are needed to understand how these fungi overcome resistance and to determine the range of available resistance genes. The development of genomic resources for these fungi and their comparison has released a torrent of new ideas and approaches to use this information to assist pathologists and agriculture in general. The sequencing of gene transcripts and the analysis of proteins from haustoria has yielded candidate virulence factors among which could be defence-triggering avirulence genes. Genome-wide computational analyses, including genetic mapping and transcript analyses by RNA sequencing of many fungal isolates, will predict many more candidates (Bakkeren et al., 2012)
Dissecting the mechanisms of host-pathogen systems like wheat-rust, including pathogen counter-defenses will ensure a step ahead towards understanding current outcomes of interactions from a co-evolutionary point of view, and eventually move a step forward in building more durable strategies for management of diseases caused by fungi (Hadrami et al.,2012)
Functional Genomics of Plant Pathogen interactions in Wheat Rust PathosystemSenthil Natesan
Cereal rust fungi are pathogens of major importance to agriculture, threatening cereal production worldwide. Targeted breeding for resistance, based on information from fungal surveys and population structure analyses of virulence, has been effective. Nevertheless, breakdown of resistance occurs frequently and continued efforts are needed to understand how these fungi overcome resistance and to determine the range of available resistance genes. The development of genomic resources for these fungi and their comparison has released a torrent of new ideas and approaches to use this information to assist pathologists and agriculture in general. The sequencing of gene transcripts and the analysis of proteins from haustoria has yielded candidate virulence factors among which could be defence-triggering avirulence genes. Genome-wide computational analyses, including genetic mapping and transcript analyses by RNA sequencing of many fungal isolates, will predict many more candidates (Bakkeren et al., 2012)
Dissecting the mechanisms of host-pathogen systems like wheat-rust, including pathogen counter-defenses will ensure a step ahead towards understanding current outcomes of interactions from a co-evolutionary point of view, and eventually move a step forward in building more durable strategies for management of diseases caused by fungi (Hadrami et al.,2012)
Engineering of Phage-Derived Lytic Enzymes: Improving Their Potential as Antimicrobials
Carlos São-José
ID
Research Institute for Medicines (iMed.ULisboa), Faculty of Pharmacy, Universidade de Lisboa,
Av. Prof. Gama Pinto, 1649-003 Lisboa, Portugal; csaojose@ff.ul.pt; Tel.: +351-217-946-420
From sequence to phenotype: Functional genomics of the oomycete PhytophthoraSophien Kamoun
Sophien Kamoun's talk at the 2002 Gordon Research Conference "Cellular and Molecular Mycology", June 16-21, Holderness School, New Hampshire, USA. https://www.grc.org/cellular-and-molecular-mycology-conference/2002/
Microbial Pathogenesis and Host Immune ResponseQIAGEN
The research community has begun correlating the makeup of individual microbiomes with disorders and diseases such as obesity, atherosclerosis and cancer. To accomplish this, researchers must first identify and characterize these microbial communities and understand the complex immune interactions between host and pathogen. This webinar provides you with a complete overview of the microbiome, metagenomics and host-pathogen interactions. Experimental strategies, from sample to insight, which can facilitate your microbiology and immunology research, are highlighted.
Genome of Athelia rolfsii genome of ~65Mb having 20290 contigs. Annotation analysis revealed 16000 genes involved in fungicide resistance, virulence and pathogenicity along with and lethal genes.Genome have GC content 46.4%
The study of pathogenomics attempts to utilize genomic and metagenomics data gathered from high through-put technologies to understand microbe diversity and interaction as well as host-microbe interactions involved in causing the disease. Pathogenomics researchers are generating and analyzing genome sequences of diverse bacterial, oomycete, fungal and viral pathogens to identify genetic sources of virulence, understand differences observed among related pathogens, guide the development of diagnosis tools capable of discriminating among specific strains, reveal sources of host resistance and understand the dynamics of host-microbe interactions and the diseases they cause .
The Documented Health Risks of Genetically Engineered Foods (Long Version)Jack Olmsted
Content of the Presentation
Regulatory Failure: It is useful to explain how such dangerous products could have made it to the market with government approval. Several slides include quotes from formerly secret FDA documents that show how government policy was at odds with more cautious scientific opinion at the agency.
Health Risks of GMOs: This section highlights many of the adverse findings revealed through laboratory experiments and reported by farmers, doctors, and investigators. It also introduces some theoretical risks based on the current state of the science.
The Consumer Tipping Point: The final section includes a discussion of a strategy to achieve the tipping point of consumer rejection of GMOs in the US, which is the basis for our Campaign for Healthier Eating in America. The key elements needed are consumer education on GMO health risks combined with clear non-GMO choices.
The Institute for Responsible Technology http://www.responsibletechnology.org/resources/powerpoint-presentation-on-gmos
Engineering of Phage-Derived Lytic Enzymes: Improving Their Potential as Antimicrobials
Carlos São-José
ID
Research Institute for Medicines (iMed.ULisboa), Faculty of Pharmacy, Universidade de Lisboa,
Av. Prof. Gama Pinto, 1649-003 Lisboa, Portugal; csaojose@ff.ul.pt; Tel.: +351-217-946-420
From sequence to phenotype: Functional genomics of the oomycete PhytophthoraSophien Kamoun
Sophien Kamoun's talk at the 2002 Gordon Research Conference "Cellular and Molecular Mycology", June 16-21, Holderness School, New Hampshire, USA. https://www.grc.org/cellular-and-molecular-mycology-conference/2002/
Microbial Pathogenesis and Host Immune ResponseQIAGEN
The research community has begun correlating the makeup of individual microbiomes with disorders and diseases such as obesity, atherosclerosis and cancer. To accomplish this, researchers must first identify and characterize these microbial communities and understand the complex immune interactions between host and pathogen. This webinar provides you with a complete overview of the microbiome, metagenomics and host-pathogen interactions. Experimental strategies, from sample to insight, which can facilitate your microbiology and immunology research, are highlighted.
Genome of Athelia rolfsii genome of ~65Mb having 20290 contigs. Annotation analysis revealed 16000 genes involved in fungicide resistance, virulence and pathogenicity along with and lethal genes.Genome have GC content 46.4%
The study of pathogenomics attempts to utilize genomic and metagenomics data gathered from high through-put technologies to understand microbe diversity and interaction as well as host-microbe interactions involved in causing the disease. Pathogenomics researchers are generating and analyzing genome sequences of diverse bacterial, oomycete, fungal and viral pathogens to identify genetic sources of virulence, understand differences observed among related pathogens, guide the development of diagnosis tools capable of discriminating among specific strains, reveal sources of host resistance and understand the dynamics of host-microbe interactions and the diseases they cause .
The Documented Health Risks of Genetically Engineered Foods (Long Version)Jack Olmsted
Content of the Presentation
Regulatory Failure: It is useful to explain how such dangerous products could have made it to the market with government approval. Several slides include quotes from formerly secret FDA documents that show how government policy was at odds with more cautious scientific opinion at the agency.
Health Risks of GMOs: This section highlights many of the adverse findings revealed through laboratory experiments and reported by farmers, doctors, and investigators. It also introduces some theoretical risks based on the current state of the science.
The Consumer Tipping Point: The final section includes a discussion of a strategy to achieve the tipping point of consumer rejection of GMOs in the US, which is the basis for our Campaign for Healthier Eating in America. The key elements needed are consumer education on GMO health risks combined with clear non-GMO choices.
The Institute for Responsible Technology http://www.responsibletechnology.org/resources/powerpoint-presentation-on-gmos
Pulmonary Thromboembolism - etilogy, types, medical- Surgical and nursing man...VarunMahajani
Disruption of blood supply to lung alveoli due to blockage of one or more pulmonary blood vessels is called as Pulmonary thromboembolism. In this presentation we will discuss its causes, types and its management in depth.
micro teaching on communication m.sc nursing.pdfAnurag Sharma
Microteaching is a unique model of practice teaching. It is a viable instrument for the. desired change in the teaching behavior or the behavior potential which, in specified types of real. classroom situations, tends to facilitate the achievement of specified types of objectives.
TEST BANK for Operations Management, 14th Edition by William J. Stevenson, Ve...kevinkariuki227
TEST BANK for Operations Management, 14th Edition by William J. Stevenson, Verified Chapters 1 - 19, Complete Newest Version.pdf
TEST BANK for Operations Management, 14th Edition by William J. Stevenson, Verified Chapters 1 - 19, Complete Newest Version.pdf
New Directions in Targeted Therapeutic Approaches for Older Adults With Mantl...i3 Health
i3 Health is pleased to make the speaker slides from this activity available for use as a non-accredited self-study or teaching resource.
This slide deck presented by Dr. Kami Maddocks, Professor-Clinical in the Division of Hematology and
Associate Division Director for Ambulatory Operations
The Ohio State University Comprehensive Cancer Center, will provide insight into new directions in targeted therapeutic approaches for older adults with mantle cell lymphoma.
STATEMENT OF NEED
Mantle cell lymphoma (MCL) is a rare, aggressive B-cell non-Hodgkin lymphoma (NHL) accounting for 5% to 7% of all lymphomas. Its prognosis ranges from indolent disease that does not require treatment for years to very aggressive disease, which is associated with poor survival (Silkenstedt et al, 2021). Typically, MCL is diagnosed at advanced stage and in older patients who cannot tolerate intensive therapy (NCCN, 2022). Although recent advances have slightly increased remission rates, recurrence and relapse remain very common, leading to a median overall survival between 3 and 6 years (LLS, 2021). Though there are several effective options, progress is still needed towards establishing an accepted frontline approach for MCL (Castellino et al, 2022). Treatment selection and management of MCL are complicated by the heterogeneity of prognosis, advanced age and comorbidities of patients, and lack of an established standard approach for treatment, making it vital that clinicians be familiar with the latest research and advances in this area. In this activity chaired by Michael Wang, MD, Professor in the Department of Lymphoma & Myeloma at MD Anderson Cancer Center, expert faculty will discuss prognostic factors informing treatment, the promising results of recent trials in new therapeutic approaches, and the implications of treatment resistance in therapeutic selection for MCL.
Target Audience
Hematology/oncology fellows, attending faculty, and other health care professionals involved in the treatment of patients with mantle cell lymphoma (MCL).
Learning Objectives
1.) Identify clinical and biological prognostic factors that can guide treatment decision making for older adults with MCL
2.) Evaluate emerging data on targeted therapeutic approaches for treatment-naive and relapsed/refractory MCL and their applicability to older adults
3.) Assess mechanisms of resistance to targeted therapies for MCL and their implications for treatment selection
Title: Sense of Taste
Presenter: Dr. Faiza, Assistant Professor of Physiology
Qualifications:
MBBS (Best Graduate, AIMC Lahore)
FCPS Physiology
ICMT, CHPE, DHPE (STMU)
MPH (GC University, Faisalabad)
MBA (Virtual University of Pakistan)
Learning Objectives:
Describe the structure and function of taste buds.
Describe the relationship between the taste threshold and taste index of common substances.
Explain the chemical basis and signal transduction of taste perception for each type of primary taste sensation.
Recognize different abnormalities of taste perception and their causes.
Key Topics:
Significance of Taste Sensation:
Differentiation between pleasant and harmful food
Influence on behavior
Selection of food based on metabolic needs
Receptors of Taste:
Taste buds on the tongue
Influence of sense of smell, texture of food, and pain stimulation (e.g., by pepper)
Primary and Secondary Taste Sensations:
Primary taste sensations: Sweet, Sour, Salty, Bitter, Umami
Chemical basis and signal transduction mechanisms for each taste
Taste Threshold and Index:
Taste threshold values for Sweet (sucrose), Salty (NaCl), Sour (HCl), and Bitter (Quinine)
Taste index relationship: Inversely proportional to taste threshold
Taste Blindness:
Inability to taste certain substances, particularly thiourea compounds
Example: Phenylthiocarbamide
Structure and Function of Taste Buds:
Composition: Epithelial cells, Sustentacular/Supporting cells, Taste cells, Basal cells
Features: Taste pores, Taste hairs/microvilli, and Taste nerve fibers
Location of Taste Buds:
Found in papillae of the tongue (Fungiform, Circumvallate, Foliate)
Also present on the palate, tonsillar pillars, epiglottis, and proximal esophagus
Mechanism of Taste Stimulation:
Interaction of taste substances with receptors on microvilli
Signal transduction pathways for Umami, Sweet, Bitter, Sour, and Salty tastes
Taste Sensitivity and Adaptation:
Decrease in sensitivity with age
Rapid adaptation of taste sensation
Role of Saliva in Taste:
Dissolution of tastants to reach receptors
Washing away the stimulus
Taste Preferences and Aversions:
Mechanisms behind taste preference and aversion
Influence of receptors and neural pathways
Impact of Sensory Nerve Damage:
Degeneration of taste buds if the sensory nerve fiber is cut
Abnormalities of Taste Detection:
Conditions: Ageusia, Hypogeusia, Dysgeusia (parageusia)
Causes: Nerve damage, neurological disorders, infections, poor oral hygiene, adverse drug effects, deficiencies, aging, tobacco use, altered neurotransmitter levels
Neurotransmitters and Taste Threshold:
Effects of serotonin (5-HT) and norepinephrine (NE) on taste sensitivity
Supertasters:
25% of the population with heightened sensitivity to taste, especially bitterness
Increased number of fungiform papillae
Ozempic: Preoperative Management of Patients on GLP-1 Receptor Agonists Saeid Safari
Preoperative Management of Patients on GLP-1 Receptor Agonists like Ozempic and Semiglutide
ASA GUIDELINE
NYSORA Guideline
2 Case Reports of Gastric Ultrasound
Anti ulcer drugs and their Advance pharmacology ||
Anti-ulcer drugs are medications used to prevent and treat ulcers in the stomach and upper part of the small intestine (duodenal ulcers). These ulcers are often caused by an imbalance between stomach acid and the mucosal lining, which protects the stomach lining.
||Scope: Overview of various classes of anti-ulcer drugs, their mechanisms of action, indications, side effects, and clinical considerations.
Title: Sense of Smell
Presenter: Dr. Faiza, Assistant Professor of Physiology
Qualifications:
MBBS (Best Graduate, AIMC Lahore)
FCPS Physiology
ICMT, CHPE, DHPE (STMU)
MPH (GC University, Faisalabad)
MBA (Virtual University of Pakistan)
Learning Objectives:
Describe the primary categories of smells and the concept of odor blindness.
Explain the structure and location of the olfactory membrane and mucosa, including the types and roles of cells involved in olfaction.
Describe the pathway and mechanisms of olfactory signal transmission from the olfactory receptors to the brain.
Illustrate the biochemical cascade triggered by odorant binding to olfactory receptors, including the role of G-proteins and second messengers in generating an action potential.
Identify different types of olfactory disorders such as anosmia, hyposmia, hyperosmia, and dysosmia, including their potential causes.
Key Topics:
Olfactory Genes:
3% of the human genome accounts for olfactory genes.
400 genes for odorant receptors.
Olfactory Membrane:
Located in the superior part of the nasal cavity.
Medially: Folds downward along the superior septum.
Laterally: Folds over the superior turbinate and upper surface of the middle turbinate.
Total surface area: 5-10 square centimeters.
Olfactory Mucosa:
Olfactory Cells: Bipolar nerve cells derived from the CNS (100 million), with 4-25 olfactory cilia per cell.
Sustentacular Cells: Produce mucus and maintain ionic and molecular environment.
Basal Cells: Replace worn-out olfactory cells with an average lifespan of 1-2 months.
Bowman’s Gland: Secretes mucus.
Stimulation of Olfactory Cells:
Odorant dissolves in mucus and attaches to receptors on olfactory cilia.
Involves a cascade effect through G-proteins and second messengers, leading to depolarization and action potential generation in the olfactory nerve.
Quality of a Good Odorant:
Small (3-20 Carbon atoms), volatile, water-soluble, and lipid-soluble.
Facilitated by odorant-binding proteins in mucus.
Membrane Potential and Action Potential:
Resting membrane potential: -55mV.
Action potential frequency in the olfactory nerve increases with odorant strength.
Adaptation Towards the Sense of Smell:
Rapid adaptation within the first second, with further slow adaptation.
Psychological adaptation greater than receptor adaptation, involving feedback inhibition from the central nervous system.
Primary Sensations of Smell:
Camphoraceous, Musky, Floral, Pepperminty, Ethereal, Pungent, Putrid.
Odor Detection Threshold:
Examples: Hydrogen sulfide (0.0005 ppm), Methyl-mercaptan (0.002 ppm).
Some toxic substances are odorless at lethal concentrations.
Characteristics of Smell:
Odor blindness for single substances due to lack of appropriate receptor protein.
Behavioral and emotional influences of smell.
Transmission of Olfactory Signals:
From olfactory cells to glomeruli in the olfactory bulb, involving lateral inhibition.
Primitive, less old, and new olfactory systems with different path
Explore natural remedies for syphilis treatment in Singapore. Discover alternative therapies, herbal remedies, and lifestyle changes that may complement conventional treatments. Learn about holistic approaches to managing syphilis symptoms and supporting overall health.
3. Innate ImmunityInnate Immunity
Defensive mechanisms include :Defensive mechanisms include :
1) Innate immunity1) Innate immunity (Natural or Non specific)(Natural or Non specific)
2) Acquired immunity2) Acquired immunity (Adaptive or Specific(Adaptive or Specific))
Cell-mediated immunity HumoralCell-mediated immunity Humoral
immunityimmunity
4. Component of Innate ImmunityComponent of Innate Immunity
Innate Immune systemInnate Immune system
First lineFirst line Second lineSecond line
1) Mechanical barriers A- cells1) Mechanical barriers A- cells
2) Chemical & biochemical inhibitors 1- Natural killer2) Chemical & biochemical inhibitors 1- Natural killer
3) Normal flora 2- Phagocytes3) Normal flora 2- Phagocytes
B- Soluble factorsB- Soluble factors
C- InflammatoryC- Inflammatory
barriersbarriers
5. First lineFirst line
1) Mechanical barriers1) Mechanical barriers
- Intact skin- Intact skin
- Mucous coat- Mucous coat
- Mucous secretion- Mucous secretion
- Blinking reflex and tears- Blinking reflex and tears
- The hair at the nares- The hair at the nares
- Coughing and sneezing reflex- Coughing and sneezing reflex
6. First lineFirst line
2) Chemical & biochemical inhibitors2) Chemical & biochemical inhibitors
- Sweet and sebaceous secretion- Sweet and sebaceous secretion
- Hydrolytic enzymes in saliva- Hydrolytic enzymes in saliva
- HCl of the stomach- HCl of the stomach
- Proteolytic enzyme in small intestine- Proteolytic enzyme in small intestine
- Lysozyme in tears- Lysozyme in tears
- Acidic pH in the adult vagina- Acidic pH in the adult vagina
7. First lineFirst line
3) Normal bacterial flora3) Normal bacterial flora
- Competition for essential- Competition for essential
nutrientsnutrients
- Production of inhibitory- Production of inhibitory
substancessubstances
8. Second lineSecond line
A) cellsA) cells
1- Natural killer (NK)1- Natural killer (NK)
Definition:Definition: Large granular lymphocytesLarge granular lymphocytes
Innate cytotoxic lymphocytesInnate cytotoxic lymphocytes
SourceSource :: Bon marrow precursorsBon marrow precursors
LocationLocation :: 10% or 15% of lymphocytes in10% or 15% of lymphocytes in peripheral bloodperipheral blood
1% or 2% of lymphocytes in1% or 2% of lymphocytes in spleenspleen
Tumor cellsTumor cells
FunctionFunction :: Cytotoxic for Viral infected cellsCytotoxic for Viral infected cells
Bacterial, fungal, parasiticBacterial, fungal, parasitic
infectioninfection
Responsible for antibody–dependent cellResponsible for antibody–dependent cell
9. Second lineSecond line
2- Phagocytes2- Phagocytes
Specialized cells for capture, Ingestion and destructionSpecialized cells for capture, Ingestion and destruction
of invading microorganismsof invading microorganisms
* Polymorphoniclear leucocytes, mainly* Polymorphoniclear leucocytes, mainly neutrophils:neutrophils:
granulocytes circulate in bloodgranulocytes circulate in blood
** Mononuclear cells (Mononuclear cells (macrophages)macrophages)
-- MonocytesMonocytes in bloodin blood
- Histocytes- Histocytes in connective tissuesin connective tissues
-- Fixed reticuloendothelial cellsFixed reticuloendothelial cells in liver spleen,in liver spleen,
lymphlymph
10. Second lineSecond line
B- Soluble factorsB- Soluble factors
1- Acute phase protein1- Acute phase protein (Plasma protein,(Plasma protein,
CRP=C reactive protein, Fibrin.)CRP=C reactive protein, Fibrin.)
2- Complement2- Complement (proteins in serum,(proteins in serum,
body fluids)body fluids)
2- Interferons2- Interferons (Proteins against viral(Proteins against viral
infections)infections)
3- Properdin3- Properdin (Complement(Complement
activation)activation)
4- Beta lysine4- Beta lysine (Antibacterial protein(Antibacterial protein
from Platelets)from Platelets)
11. InterferonsInterferons
Proteins usually produced by virally infected cellsProteins usually produced by virally infected cells
* Types of interferons:* Types of interferons:
1- Alpha interferon1- Alpha interferon Secreted by MacrophagesSecreted by Macrophages
Induced by Viruses or PolynucleotideInduced by Viruses or Polynucleotide
2- Beta interferon2- Beta interferon Secreted by Fibroblasts, VirusesSecreted by Fibroblasts, Viruses
3- Gamma interferon3- Gamma interferon T- lymphocytes, Specific antigensT- lymphocytes, Specific antigens
12. InterferonsInterferons
Protective action of interferons:Protective action of interferons:
1) Activate T-cells1) Activate T-cells
2) Activate macrophages2) Activate macrophages
3) Activate NK3) Activate NK
13. PhagocytosisPhagocytosis
The engulfment, digestion, and subsequent processingThe engulfment, digestion, and subsequent processing
of microorganisms by macrophages and neutrophilsof microorganisms by macrophages and neutrophils
1) Chemotaxis & attachment:1) Chemotaxis & attachment:
a- Attraction by chemotactic substancesa- Attraction by chemotactic substances
(microbes, damaged tissues)(microbes, damaged tissues)
b- Attachment by receptors on surfacesb- Attachment by receptors on surfaces
14. PhagocytosisPhagocytosis
2) Ingestion:2) Ingestion:
* Phagocyte pseudopodia surround* Phagocyte pseudopodia surround
organism forming phagosomorganism forming phagosom
* Opsinins and co-factors enhance* Opsinins and co-factors enhance
phagocytosisphagocytosis
* Fusion with phagocyte granules and* Fusion with phagocyte granules and
releaserelease
digestive, toxic contentsdigestive, toxic contents
15. PhagocytosisPhagocytosis
3- Killing (two microbicidal routes)3- Killing (two microbicidal routes)
a- Oxygen depended system (powerful microbicidala- Oxygen depended system (powerful microbicidal
agents)agents)
Oxygen converted to superoxide, anion,Oxygen converted to superoxide, anion,
hydrogen peroxide, activated oxygen andhydrogen peroxide, activated oxygen and
hydroxyl radicals.hydroxyl radicals.
b- Oxygen-independent system (anaerobicb- Oxygen-independent system (anaerobic
conditions)conditions)
Digestion and killing by lysozyme. Lactoferrin,Digestion and killing by lysozyme. Lactoferrin,
low pH, cationic proteins and hydrolytic andlow pH, cationic proteins and hydrolytic and
proteolytic enzymesproteolytic enzymes
16. C) Inflammatory BarriersC) Inflammatory Barriers
* Tissue damage by a wound or by invading pathogen* Tissue damage by a wound or by invading pathogen
* Inflammatory response:* Inflammatory response:
Tissue damageTissue damage
Release of chemical mediators fromRelease of chemical mediators from LeukocytesLeukocytes
(Histamine, fibrin, kinins, cytokines)(Histamine, fibrin, kinins, cytokines) Invading microbeInvading microbe
Redness of tissueRedness of tissue
Tissue temperatureTissue temperature
Vasodilatation of capillariesVasodilatation of capillaries Capillary permeabilityCapillary permeability
Influx of fluidsInflux of fluids
Influx of phagocytesInflux of phagocytes
into tissuesinto tissues