This paper circulates around the core theme of Leishmaniasis is a parasitic infection caused by a protozoan from the Trypanosomatidae family, genus Leishmania. A well established mouse model of visceral leismaniasis disease exists using a strain (BALB/C) of mice susceptible to the disease together with its essential aspects. It has been reviewed and purchased by the majority of students thus, this paper is rated 4.8 out of 5 points by the students. In addition to this, the price of this paper commences from £ 99. To get this paper written from the scratch, order this assignment now. 100% confidential, 100% plagiarism-free.
In course Assessment
Leishmaniasis is a parasitic infection caused by a protozoan from the Trypanosomatidae family, genus Leishmania. A well established mouse model of visceral leismaniasis disease exists using a strain (BALB/C) of mice susceptible to the disease. An experiment was performed in order to examine the effects of an anti- IL-10 immunomodulatory agent on cytokine production by T cells in a mouse model of Leismaniasis. L. major promastigotes were injected into the ears of BALB/c mice.
After 4 weeks T cells were isolated from the lymph nodes and cultured for 48 hours in the presence of 5 μg/mL of soluble Leishmania antigen (SLA). Supernatants from these cultures were harvested and ELISA experiments performed to investigate IFNg and IL-4 production by the T cells. Following infection, a group of mice were treated with an anti-IL-10 immunomodulatory agent prior to isolation and culture of T cells.
For comparison, two groups of control mice were used: one group was uninfected and untreated (no immunomodulatory agent) and the other was uninfected but treated with the anti-IL-10 agent. Details of the samples can be found below. Following infection, L.major infected mice developed skin lesions and showed a high worm burden at the site of infection. The anti-IL-10 treated mice showed reduced
symptoms and reduced worm burden. Both groups of control mice were healthy.
Sample A = Untreated mouse.
Sample B = L.major infected mouse.
Sample C = L.major infected mouse treated with anti-IL-10.
Sample D = Uninfected mice treated with anti-IL-10 alone.
Samples were added to ELISA plates in the following layout – and the raw absorbance data is
indicated for each cytokine.
Task:
You should first analyse the data you are provided with to determine the amount of IFNg and IL-4 produced by each of the four experimental samples (A-D).
a) You should plot the standard curve of the two ELISA experiments on a graph using an appropriate analysis package (eg. Sigmaplot, etc) – ensure graphs are presented and labelled appropriately.
b) You should present the results of your analysis of the experimental samples in a separate graph.
c) You should describe your results (500 words maximum). Remember to include a description of what your sample and treatment groups did in comparison to controls. You should comment on what the sensitivity of the two ELISA experiments was and how significant, reliable and reproducible your results are.
d) You should then give a brief discussion and conclusion for your findings (500 words maximum). Why were these two cytokines measured? What can they tell us about how the body fights the infection? Why might treatment with the anti-IL-10 agent effect the production of IFNg and IL-4 by T cells and why might this effect the health of the mice. Finally, can you find any research
literature that supports these conclusions in human Leismaniasis infection?
