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Peter C Doherty
was born in the town of
Brisbane and his early school
life was spent attending the
Indooroopilly state high
school. Peter joined the John
Curtin School of Medical
Research in Canberra in 1972
where he met Rolf M.
Zinkernagel, Doherty then
went on to teach at the Wistar
Institute in Philadelphia
between the years of 1975-
1982. Between the years of
1982-1988, Doherty headed
the department of Pathology
at the Curtin School in
Canberra. Doherty currently
splits his time between
researching at St Jude
Children’s Research Hospital in
Tennessee and working in the
Department of Microbiology.
(Britannica, 2016)
Dr Peter Doherty’s
research was all
about looking at how the
body got rid of viral infections
by observing Killer T cells in
mice. Bob Blanden at the
John Curtin School of Medical
Research was researching the
cytotoxic T-cell response,
however after Bob’s lab got
crowded Zinkernagel moved
into Doherty’s lab. After a
while of being in the same lab
Rolf Zinkernagel and Doherty
began collaborating. The two
then discovered T-cells in mice
infected with a lymphocytic
virus called LCMV in which
they were able to get these
cells to attack the cells
infected with the virus.
(AAS, 2016).
General Virus Information
The SOV (2014) state how the immune system destroys
the microbes faster if they enter the body for a second
time, due to the fact that the body recognises them
from previous experience and destroys them before
they multiply. Viral antigens like this are present
everywhere in body, depending on the rate and phase
of infection will determine where they spread to,
however they are not necessarily a systemic immunity.
Klimpel (1996) describes how the existence of a variety
of defences is not surprising due to the diversity, hosts,
body compartments, cells and mechanisms of virus
multiplication. ELSEVIER (2006) states how the immune
system recognizes virus-infected cells through
mechanisms that are not antigen-specific, the cytokines
produced during early phase of the host’s defence do
facilitate activation of subsequent antigen-specific
adaptive immune mechanisms.
Matt
Mice were infected with influenza
virus, which was found to grow in
epithelial cells of respiratory tract. This is
the only place the virus successfully
grew.
Production of Cytokines causes a large
recruitment of cells into affected area in order to
recruit precursor cells which recognize cells infected
with the influenza virus, precursor cells then replicate
and become effective T-cells which then move
back to the virus infected area and kill of the
virus.
Virus was found to move into dendritic cells
of the upper respiratory tract, Dendritic cells
present as the ideal androgen presenting cells for
T-cell stimulation, The dendritic cells then carry viral
peptides, viral mRNA and viral DNA to the lymph
nodes in the throat causing inflammation.
(Inflammation caused by production of
cytokines)
References:- AAS. (2016). Professor Peter Doherty, immunologist. Retrieved from https://www.science.org.au/learning/general-
audience/history/interviews-australian-scientists/professor-peter-doherty#2
- Alberts, B., Johnson, A., Lewis, J., Raff, M., Roberts, K., & Walter, P. (2002). T cells and MHC proteins. Retrieved from
http://www.ncbi.nlm.nih.gov/books/NBK26926/
- C, P. (1996). Nobel lecture by peter C. Doherty (50 minutes). Retrieved May 2, 2016, from Nobel Prize,
http://www.nobelprize.org/mediaplayer/index.php?id=1710
- Doherty, P. C. (2007). Challenged by complexity: My Twentieth century in immunology. Annual Review of Immunology, 25(1),
1–19. doi:10.1146/annurev.immunol.25.022106.141644
- DOHERTY, P. C. (2010). ChemInform abstract: Cell-mediated immunity in virus infections (Nobel lecture). ChemInform, 28(50),
no–no. doi:10.1002/chin.199750334
- ELSEVIER (2006). The immune response to influenza infection - article in motion. Retrieved May 8, 2016, from Elsevier,
http://www.rapidreferenceinfluenza.com/chapter/B978-0-7234-3433-7.50011-6/aim/introduction
- Encyclopædia Britannica, I. (2015). Retrieved from Peter C. Doherty: http://www.britannica.com/biography/Peter-C-Doherty
- Klimpel, G. R. (1996). Immune defenses. Retrieved from http://www.ncbi.nlm.nih.gov/books/NBK8423/
- Nobelprize.org. Nobel Media AB 2014. Web. 2 May 2016. http://www.nobelprize.org/mediaplayer/index.php?id=1710
- State of Victoria (SOV). (2014, March 31). Immune system. Retrieved May 8, 2016, from Immune System,
https://www.betterhealth.vic.gov.au/health/conditionsandtreatments/immune-system
- Winslow, T. (2016, April 27). 6. Autoimmune diseases and the promise of stem cell-based therapies [Stem cell Information].
Retrieved April 28, 2016, from Stem Cell Information, http://stemcells.nih.gov/info/scireport/pages/chapter6.aspx
Figure 3 (Background):
Fiona Macrae Science Editor In Washington D.c. (2016). Stunning new therapy hunts down and destroys cancer cells. Daily Mail.
Retrieved 8 May 2016, from http://www.dailymail.co.uk/health/article-3448598/The-living-drug-wipe-cancer-Stunning-new-
therapy-hunts-destroys-diseased-cells-prevents-returning.html
Doherty began his research with the ideas on how
the virus molecule and the histocompatibility protein
molecule, would focus on the surface of a cell and
then altered it, Doherty (2007) states that he and
Zinkernagel’s first experiment viewed this through
whether or not an infected mouse brain contained
CTL effectors. This began through the studies of Paul
Ehrlich, Doherty (2010) found in his research that
through Evans blue injections a mice brain would
show how the brain breaks down along with the
blood brain barrier due to the virus within the dye.
Doherty (1996) states that when the virus is injected
the t cell response kills the virus consequently making
the brain swell, because protein floods into the brain
and the brain can't stand the unbalanced
osmolality and the amount of cerebrospinal fluid
that is needed decreases. This influenced Doherty to
do complex experiments and according to ACC
(2015) they concluded that T
cells have to focus onto the virus
infected cell in the body,
allowing helper T cells to find
the virus infected cell and kill it.
As seen in figure 2 all of this is
possible through Doherty’s
gained knowledge of white
blood cells, including T
and B lymphocytes the three
main T cells, cytotoxic,
helper and an memory.
- MHC (major histocompatibility
complex) molecules are normal
components of healthy cells.
- Helped the immune system to
recognize microorganisms other
than viruses, and react against
certain kinds of self-tissues.
- Doherty and
Zinkernagel
immunized
mice with a
virus causing
meningitis.
- They isolated
the immune T-
killer cells, and
found that they
had to
recognize two
things on the
surface of the
infected cells in
order to kill
them.
Figure 1:
Zinkernagel, R. M., & Doherty, P. C. (1997b). The discovery of MHC
restriction. Immunology Today. Elsevier BV
Figure 2:
Kimbal Biology. (2011). Cytotoxic T
lymphocytes (CTL). Retrieved 2 May 2016, from
http://www.biology-pages.info/C/CTL.html
Experiment process
Discoveries
How it all worked
1
2
3

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final poster

  • 1. Peter C Doherty was born in the town of Brisbane and his early school life was spent attending the Indooroopilly state high school. Peter joined the John Curtin School of Medical Research in Canberra in 1972 where he met Rolf M. Zinkernagel, Doherty then went on to teach at the Wistar Institute in Philadelphia between the years of 1975- 1982. Between the years of 1982-1988, Doherty headed the department of Pathology at the Curtin School in Canberra. Doherty currently splits his time between researching at St Jude Children’s Research Hospital in Tennessee and working in the Department of Microbiology. (Britannica, 2016) Dr Peter Doherty’s research was all about looking at how the body got rid of viral infections by observing Killer T cells in mice. Bob Blanden at the John Curtin School of Medical Research was researching the cytotoxic T-cell response, however after Bob’s lab got crowded Zinkernagel moved into Doherty’s lab. After a while of being in the same lab Rolf Zinkernagel and Doherty began collaborating. The two then discovered T-cells in mice infected with a lymphocytic virus called LCMV in which they were able to get these cells to attack the cells infected with the virus. (AAS, 2016). General Virus Information The SOV (2014) state how the immune system destroys the microbes faster if they enter the body for a second time, due to the fact that the body recognises them from previous experience and destroys them before they multiply. Viral antigens like this are present everywhere in body, depending on the rate and phase of infection will determine where they spread to, however they are not necessarily a systemic immunity. Klimpel (1996) describes how the existence of a variety of defences is not surprising due to the diversity, hosts, body compartments, cells and mechanisms of virus multiplication. ELSEVIER (2006) states how the immune system recognizes virus-infected cells through mechanisms that are not antigen-specific, the cytokines produced during early phase of the host’s defence do facilitate activation of subsequent antigen-specific adaptive immune mechanisms. Matt Mice were infected with influenza virus, which was found to grow in epithelial cells of respiratory tract. This is the only place the virus successfully grew. Production of Cytokines causes a large recruitment of cells into affected area in order to recruit precursor cells which recognize cells infected with the influenza virus, precursor cells then replicate and become effective T-cells which then move back to the virus infected area and kill of the virus. Virus was found to move into dendritic cells of the upper respiratory tract, Dendritic cells present as the ideal androgen presenting cells for T-cell stimulation, The dendritic cells then carry viral peptides, viral mRNA and viral DNA to the lymph nodes in the throat causing inflammation. (Inflammation caused by production of cytokines) References:- AAS. (2016). Professor Peter Doherty, immunologist. Retrieved from https://www.science.org.au/learning/general- audience/history/interviews-australian-scientists/professor-peter-doherty#2 - Alberts, B., Johnson, A., Lewis, J., Raff, M., Roberts, K., & Walter, P. (2002). T cells and MHC proteins. Retrieved from http://www.ncbi.nlm.nih.gov/books/NBK26926/ - C, P. (1996). Nobel lecture by peter C. Doherty (50 minutes). Retrieved May 2, 2016, from Nobel Prize, http://www.nobelprize.org/mediaplayer/index.php?id=1710 - Doherty, P. C. (2007). Challenged by complexity: My Twentieth century in immunology. Annual Review of Immunology, 25(1), 1–19. doi:10.1146/annurev.immunol.25.022106.141644 - DOHERTY, P. C. (2010). ChemInform abstract: Cell-mediated immunity in virus infections (Nobel lecture). ChemInform, 28(50), no–no. doi:10.1002/chin.199750334 - ELSEVIER (2006). The immune response to influenza infection - article in motion. Retrieved May 8, 2016, from Elsevier, http://www.rapidreferenceinfluenza.com/chapter/B978-0-7234-3433-7.50011-6/aim/introduction - Encyclopædia Britannica, I. (2015). Retrieved from Peter C. Doherty: http://www.britannica.com/biography/Peter-C-Doherty - Klimpel, G. R. (1996). Immune defenses. Retrieved from http://www.ncbi.nlm.nih.gov/books/NBK8423/ - Nobelprize.org. Nobel Media AB 2014. Web. 2 May 2016. http://www.nobelprize.org/mediaplayer/index.php?id=1710 - State of Victoria (SOV). (2014, March 31). Immune system. Retrieved May 8, 2016, from Immune System, https://www.betterhealth.vic.gov.au/health/conditionsandtreatments/immune-system - Winslow, T. (2016, April 27). 6. Autoimmune diseases and the promise of stem cell-based therapies [Stem cell Information]. Retrieved April 28, 2016, from Stem Cell Information, http://stemcells.nih.gov/info/scireport/pages/chapter6.aspx Figure 3 (Background): Fiona Macrae Science Editor In Washington D.c. (2016). Stunning new therapy hunts down and destroys cancer cells. Daily Mail. Retrieved 8 May 2016, from http://www.dailymail.co.uk/health/article-3448598/The-living-drug-wipe-cancer-Stunning-new- therapy-hunts-destroys-diseased-cells-prevents-returning.html Doherty began his research with the ideas on how the virus molecule and the histocompatibility protein molecule, would focus on the surface of a cell and then altered it, Doherty (2007) states that he and Zinkernagel’s first experiment viewed this through whether or not an infected mouse brain contained CTL effectors. This began through the studies of Paul Ehrlich, Doherty (2010) found in his research that through Evans blue injections a mice brain would show how the brain breaks down along with the blood brain barrier due to the virus within the dye. Doherty (1996) states that when the virus is injected the t cell response kills the virus consequently making the brain swell, because protein floods into the brain and the brain can't stand the unbalanced osmolality and the amount of cerebrospinal fluid that is needed decreases. This influenced Doherty to do complex experiments and according to ACC (2015) they concluded that T cells have to focus onto the virus infected cell in the body, allowing helper T cells to find the virus infected cell and kill it. As seen in figure 2 all of this is possible through Doherty’s gained knowledge of white blood cells, including T and B lymphocytes the three main T cells, cytotoxic, helper and an memory. - MHC (major histocompatibility complex) molecules are normal components of healthy cells. - Helped the immune system to recognize microorganisms other than viruses, and react against certain kinds of self-tissues. - Doherty and Zinkernagel immunized mice with a virus causing meningitis. - They isolated the immune T- killer cells, and found that they had to recognize two things on the surface of the infected cells in order to kill them. Figure 1: Zinkernagel, R. M., & Doherty, P. C. (1997b). The discovery of MHC restriction. Immunology Today. Elsevier BV Figure 2: Kimbal Biology. (2011). Cytotoxic T lymphocytes (CTL). Retrieved 2 May 2016, from http://www.biology-pages.info/C/CTL.html Experiment process Discoveries How it all worked 1 2 3