Blood stage malaria antigens induce different activation-induced cell death programs in splenic CD4+T cells.

Abstract:

:CD4(+) T cells respond to antigen immunization through a process of activation, clonal expansion to generate activated effector T cells followed by activation-induced clonal deletion of the responding T cells. While loss of responding T cells in post-activation death by apoptosis is a major factor regulating immune homeostasis, the precise pathways involved in downsizing of Plasmodium falciparum antigen-induced T cell expansions are not well characterized. We report in this study that splenic CD4(+) T cells from mice immunized with nonreplicating immunogens like OVA or recombinant blood stage P. falciparum antigens, PfMSP-3 and PfMSP-1(19) or crude parasite antigen (PfAg) undergo sequential T cell activation, proliferation followed by activation-induced cell death (AICD) in a dose- and time-dependent manner after Ag restimulation. While PfMSP-3 and OVA-induced AICD was mediated through a death receptor-dependent apoptotic program, PfMSP-1(19) and PfAg-induced AICD was via a mechanism dependent on the activation of mitochondria apoptosis signalling pathway through Bax activation. These results provide insights into the mechanism through which two blood stage merozoite antigens trigger different apoptotic programs of AICD in splenic CD4(+) T cells.

journal_name

Parasite Immunol

journal_title

Parasite immunology

authors

Mukherjee P,Devi YS,Chauhan VS

doi

10.1111/j.1365-3024.2008.01050.x

subject

Has Abstract

pub_date

2008-10-01 00:00:00

pages

497-514

issue

10

eissn

0141-9838

issn

1365-3024

pii

PIM1050

journal_volume

30

pub_type

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