Meding S J, Langhorne J
Max-Planck-Institute für Immunbiologie, Freiburg, FRG.
Eur J Immunol. 1991 Jun;21(6):1433-8. doi: 10.1002/eji.1830210616.
It is shown here that B cells, in addition to CD4+ T cells, are necessary for the development of protective immunity to Plasmodium chabaudi chabaudi (P. chabaudi) in mice. Reconstitution of severe combined immunodeficient (SCID) mice with immune or normal CD4+ T cells protected the majority of mice against an otherwise lethal challenge but the mice were unable to clear their parasitemias. By contrast, transfer of the same T cell populations into athymic nu/nu mice enabled the recipients to control and clear their infections, immune CD4+ T cells being most effective. Furthermore, SCID mice given CD4+ T cells from immune and normal donors simultaneously with immune B cells also could eliminate their infection. Clearance of parasitemia correlated with the presence of malaria-specific antibodies in the serum. The role of B cells and CD4+ T cells in the protective immune response to P. chabaudi is discussed.
本文表明,除CD4+ T细胞外,B细胞对于小鼠产生针对恰氏疟原虫(P. chabaudi)的保护性免疫也是必需的。用免疫或正常的CD4+ T细胞重建严重联合免疫缺陷(SCID)小鼠,可保护大多数小鼠免受原本致命的攻击,但这些小鼠无法清除其体内的寄生虫血症。相比之下,将相同的T细胞群体转移到无胸腺裸鼠体内,使受体能够控制并清除感染,免疫CD4+ T细胞最为有效。此外,同时给予来自免疫和正常供体的CD4+ T细胞以及免疫B细胞的SCID小鼠也能够消除感染。寄生虫血症的清除与血清中疟疾特异性抗体的存在相关。文中讨论了B细胞和CD4+ T细胞在针对恰氏疟原虫的保护性免疫反应中的作用。