Genetic control of schistosome infections by the SM1 locus of the 5q31-q33 region is linked to differentiation of type 2 helper T lymphocytes

被引:45
作者
Rodrigues, V
Piper, K
Couissinier-Paris, P
Bacelar, O
Dessein, H
Dessein, AJ
机构
[1] Univ Mediterranee, INSERM, U399, Fac Med Marseille, F-13385 Marseille 5, France
[2] Fac Med Triangulo Mineiro, Lab Imunol, BR-38025160 Uberaba, MG, Brazil
关键词
D O I
10.1128/IAI.67.9.4689-4692.1999
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Human susceptibility to Schistosoma mansoni infections is controlled by the SM1 locus on chromosome 5 in q31-q33, This genetic region encodes cytokines which regulate the development of helper T lymphocytes, In the present work, a clonal analysis of CD4(+) T lymphocytes of homozygous resistant and homozygous susceptible subjects was undertaken to evaluate whether SM1 controls helper T-cell differentiation. Of 121 CD4(+) T-cell clones (TCC) from three susceptible (S) and three resistant (R) subjects, 68 proliferated when stimulated by parasite antigens, Parasite-specific TCC derived from susceptible subjects (33 STCC) produced 10- to 1,000-fold less interleukin-4 acid -5 than TCC from resistant subjects (25 RTCC). Clones from both patient groups produced, however, the same amount of gamma interferon. Parasite-specific STCC were type 1 helper (Th1) or Th0/1, whereas RTCC were either Th2 or Th0/2. These results, together with the localization of SM1 in 5q31-q33, indicate that the SM1 locus controls the differentiation of Th2 lymphocytes.
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收藏
页码:4689 / 4692
页数:4
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