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ResultsPhenotypic profile of shortterm cell lines

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CD8 T cells were stimulated in 2 out of the 3 ... Nester, Eugene W., C. Evans Roberts, Nancy N. Pearsall, Denise G. Anderson, and ... Steinman, Lawrence. 1996. ... – PowerPoint PPT presentation

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Title: ResultsPhenotypic profile of shortterm cell lines


1
Results-Phenotypic profile of short-term cell
lines
2
Conclusion-Figure 3.
  • CD8 T cells were stimulated in 2 out of the 3
    patients
  • Phenotype of responding cells differed depending
    on the vaccine clones used
  • Overall cytokine response was seen from TCR-ab
  • All the clones stimulated Natural Killer cells

3
Rationale-Figure 4.
  • To determine the type of immune response that is
    generated by T cell vaccination
  • Non-stimulated and stimulated PBMC cultures were
    studied all in vitro

4
Figure 4.-Cytokine Production Profile
5
Conclusion-Figure 4.
  • Controls PBMC cultures did not produce IL-4
  • Some control cases showed low levels of IFN-g
  • IFN-g and TNF-a production was observed in most
    cultures
  • IFN-g production increased in most patients after
    the 3rd vaccination

6
Rationale-Figure 5.
  • To study the relative contributions of CD4,
    CD8, and gd T cells to cytokine production after
    vaccination
  • Certain T cells were removed from the PBMC
  • Controls were PBMC containing all T cells
  • Depleted cell mixtures were irradiated in vitro
    with vaccine cells
  • Results were obtained using flowcytometry

7
Figure 5.-Proliferation and cytokine production
of depleted PBMC
8
Conclusion-Figure 5.
  • CD4 cells most often reduced proliferation
  • Depletion of CD8 T cells did not greatly alter
    proliferation
  • In some cases, gd T cell depletion raised
    proliferative activity
  • Depletion of gd T cells did not have a major
    effect on cytokine production
  • The major effector of cytokine production was
    CD4 T cells

9
Conclusion
  • Precise mechanisms by which T cell vaccination
    ameliorates autoimmune disease are still unclear
  • The majority of patients the proliferative
    response was maximal after the 2nd and 3rd
    vaccinations
  • For long term T cell response, SI units greater
    than 2 were observed in at least one clones for
    all patients (See Figure 2) indicating there may
    be memory antigen-specific lymphocytes

10
Conclusion Contd
  • From Figure 3., it is concluded that the
    phenotypic characteristics obtained after
    stimulation with vaccine cell lines demonstrate
    that CD4/- and CD8/- cells respond to the
    vaccine
  • Figure 4., reinerates the fact that cytokine
    production increased mainly after the 3rd
    vaccination
  • Depletion of CD4 T cells led to a substanial
    reduction in proliferative response indictaing
    CD4 T cells role to vaccine responses in vitro

11
References
  • Hermans, Guy, Ulrike Denzer, Ansgar Lohse, Jef
    Raus, and Piet Stinissen. 1999. Cellular and
    Humoral Immune Responses Against Autoreactive T
    cells in Multiple Sclerosis Patients After T cell
    Vaccination. Journal of Autoimmunity 13
    233-246.
  • Nester, Eugene W., C. Evans Roberts, Nancy N.
    Pearsall, Denise G. Anderson, and Martha T.
    Nester. 1998. Microbiology A Human
    Perspective. 2nd edition. Boston WCB
    McGraw-Hill. 367-370pp.
  • Pouly, Sandrine and Jack P. Antel. 1999.
    Multiple Sclerosis and Central Nervous System
    Demyelination. Journal of Autoimmunity
    13297-306.
  • Steinman, Lawrence. 1996. Multiple Sclerosis A
    Coordinated Immunological Attack against Myelin
    in the Central Nervous System. Nature 365
    642-644.
  • http//mail.med.upenn.edu/hessd/Lesson2.html
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