ELEVATED CELLULAR IMMUNE-RESPONSES AND INTERFERON-GAMMA RELEASE AFTER LONG-TERM DIETHYLCARBAMAZINE TREATMENT OF PATIENTS WITH HUMAN LYMPHATIC FILARIASIS

被引:72
作者
SARTONO, E
KRUIZE, YCM
KURNIAWAN, A
VANDERMEIDE, PH
PARTONO, F
MAIZELS, RM
YAZDANBAKHSH, M
机构
[1] LEIDEN UNIV,DEPT PARASITOL,2300 RC LEIDEN,NETHERLANDS
[2] TNO,MED BIOL LAB,2280 AA RIJSWIJK,NETHERLANDS
[3] UNIV INDONESIA,DEPT PARASITOL,JAKARTA,INDONESIA
[4] UNIV LONDON IMPERIAL COLL SCI TECHNOL & MED,WELLCOME RES CTR PARASIT INFECT,DEPT BIOL,LONDON,ENGLAND
基金
英国惠康基金;
关键词
D O I
10.1093/infdis/171.6.1683
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Cellular immune responses to filarial antigens were examined in persons before and 1 year after beginning treatment with diethylcarbamazine (DEC). The subjects (17 microfilaremics, 13 asymptomatic amcirofilaremics, and 13 with elephantiasis) had not responded to Brugia malayi adult worm antigen (BmA) before chemotherapy. T cell proliferative responses to BmA improved significantly after therapy in the 3 clinical groups (P < .05) but was highest in the elephantiasis patients and asymptomatic amicrofilaremics. Cytokine release profiles after stimulation with parasite antigen were analyzed, Production of interferon (IFN)-gamma by BmA-stimulated mono-nuclear cells increased significantly after DEC treatment (geometric mean, 39.6-55.7 U/mL; P < .05), largely due to improved responses in elephantiasis patients and asymptomatic amicrofilaremics, In contrast, BmA-induced interleukin (IL)-4 release did not change significantly in these same patients after treatment. Thus, both microfilaremic and amicrofilaremic infections with B. malayi are associated with similar down-regulation of proliferative T cell function and IFN-gamma release.
引用
收藏
页码:1683 / 1687
页数:5
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