Chen W, Harp J A, Harmsen A G
Trudeau Institute, Inc., Saranac Lake, New York 12983.
Infect Immun. 1993 Sep;61(9):3928-32. doi: 10.1128/iai.61.9.3928-3932.1993.
The importance of CD4+ cells and gamma interferon (IFN-gamma) in the resolution of established Cryptosporidium parvum infection was investigated with a murine model of cryptosporidiosis in severe combined immunodeficient (SCID) mice. C. parvum-infected SCID mice were reconstituted with spleen cells from immunocompetent donors. The recipients were able to resolve their C. parvum infection by 17 days postreconstitution. Treatment of reconstituted SCID mice with either anti-CD4 monoclonal antibodies to deplete them of CD4+ cells or with anti-IFN-gamma to neutralize IFN-gamma activity reduced or eliminated their ability to resolve C. parvum infection whereas treatment with either anti-CD8 monoclonal antibodies or anti-asialo-GM1 antibodies had no effect. We also found C. parvum-specific antibodies in serum samples from two of four reconstituted SCID mice killed on postreconstitution day 17 but not in unreconstituted SCID mice. Moreover, anti-CD4-treated mice had no detectable specific antibodies to C. parvum, whereas all mice treated with either anti-CD8 or anti-asialo-GM1 had substantial levels of specific antibodies in their serum. Although the role of the specific antibody is not known, these findings clearly indicate that resolution of an established C. parvum infection in immunologically reconstituted SCID mice is dependent on both CD4+ cells and IFN-gamma.
利用重度联合免疫缺陷(SCID)小鼠隐孢子虫病的鼠模型,研究了CD4 +细胞和γ干扰素(IFN-γ)在已建立的微小隐孢子虫感染消退中的重要性。用来自免疫活性供体的脾细胞重建感染微小隐孢子虫的SCID小鼠。受体在重建后17天能够消退其微小隐孢子虫感染。用抗CD4单克隆抗体耗尽其CD4 +细胞或用抗IFN-γ中和IFN-γ活性来处理重建的SCID小鼠,会降低或消除它们消退微小隐孢子虫感染的能力,而用抗CD8单克隆抗体或抗唾液酸GM1抗体处理则没有效果。我们还在重建后第17天处死的四只重建SCID小鼠中的两只的血清样本中发现了微小隐孢子虫特异性抗体,但未在未重建的SCID小鼠中发现。此外,抗CD4处理的小鼠没有可检测到的针对微小隐孢子虫的特异性抗体,而所有用抗CD8或抗唾液酸GM1处理的小鼠血清中都有大量的特异性抗体。虽然特异性抗体的作用尚不清楚,但这些发现清楚地表明,在免疫重建的SCID小鼠中,已建立的微小隐孢子虫感染的消退依赖于CD4 +细胞和IFN-γ。