T cell responses to crude and defined leishmanial antigens in patients from the Lower Amazon region of Brazil infected with different species of Leishmania of the subgenera Leishmania and Viannia

被引:0
|
作者
Silveira, FT
Blackwell, JM
Ishikawa, EA
Braga, R
Shaw, JJ
Quinnell, RJ
Soong, L
Kima, P
McMahon-Pratt, D
Black, GF
Shaw, MA
机构
[1] Inst Evandro Chagas FNS, BR-66050 Belem, Para, Brazil
[2] Univ Cambridge, Addenbrookes Hosp, Dept Med, Sch Clin Med, Cambridge CB2 2QQ, England
[3] Univ London London Sch Hyg & Trop Med, Dept Infect & Trop Dis, London WC1E 7HT, England
[4] Yale Univ, Dept Epidemiol & Publ Hlth, New Haven, CT 06520 USA
基金
英国惠康基金;
关键词
cutaneous leishmaniasis; T cell therapy;
D O I
10.1046/j.1365-3024.1998.t01-1-00126.x
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Amazonian localized cutaneous leishmaniasis (LCL) is caused by parasites of the subgenera Leishmania and Viannia. Respectively, these parasites may cause diffuse cutaneous leishmaniasis (DCL) and mucocutaneous leishmaniasis (MCL). This, together with differing skin test responses, suggests some species-specificity in cell mediated immunity. In this study, T cell responses (proliferative and interferon-gamma) to crude and defined antigens were examined in paired samples pre and post chemotherapy. Untreated L. L.) amazonensis LCL patients showed lower responses to crude leishmanial antigens than the L. (V.) spp. group. L, (V.) braziliensis antigen was a more potent stimulator of T cell responses than L. (L.) amazonensis antigen in all patient groups. Few positive responses were seen to the L. (L.) amazonensis glycoprotein GP46. A substantial proportion of LCL patients did respond to the L. (L.) pifanoi amastigote antigens A2, and the surface membrane glycoprotein P8. DCL patients were poor responders to all leishmanial antigens, except GP46. In. contrast MCL patients were good responders to all antigens except GP46 and A2. A significant rise in the response to P8 and A2 antigen was seen post treatment across all LCL and MCL patients, indicating that these antigens might provide suitable vaccine candidates.
引用
收藏
页码:19 / 26
页数:8
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