Abstract:
:CBA/J mice are resistant to Leishmania major and susceptible to Leishmania amazonensis. Early events determine infection outcome. Until now, PIV (in vitro priming) immune response to L. amazonensis has not been assessed. Herein, we have shown that compared to L. major, L. amazonensis induced higher parasite burden associated to similar IL-4, IFN-gamma, and TNF-alpha mRNA expressions and IFN-gamma and IL-10 levels. Although similar amounts of IL-10 were detected, the frequency of intracellular IL-10 positive B cells was enhanced in spleen cells stimulated with anti-CD3/anti-CD28, or anti-CD3/anti-CD28 and L. amazonensis, compared to L. major-stimulation. Interestingly, IL-10- producing B cells were reduced in response to anti-CD3/anti-CD28 stimulation combined with L. major compared to the other groups. L. amazonensis may favor T regulatory cell development, since 40% of all the CD4+CD25+ were CD25(high) cells. These data suggest that in PIV, susceptibility to L. amazonensis is not related to Th cell polarization, but to the presence and activity of regulatory T and B cells.
journal_name
Exp Parasitoljournal_title
Experimental parasitologyauthors
Veras PS,Welby-Borges M,de Santana CD,Nihei J,Cardillo F,de Freitas LAdoi
10.1016/j.exppara.2006.01.008keywords:
subject
Has Abstractpub_date
2006-07-01 00:00:00pages
201-5issue
3eissn
0014-4894issn
1090-2449pii
S0014-4894(06)00009-9journal_volume
113pub_type
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