Nussbaum G, Yuan R, Casadevall A, Scharff M D
Department of Cell Biology, Albert Einstein College of Medicine, Bronx, New York 10461, USA.
J Exp Med. 1996 Apr 1;183(4):1905-9. doi: 10.1084/jem.183.4.1905.
Vaccination and infection can elicit protective and nonprotective antibodies to the fungus Cryptococcus neoformans in mice. The effect of nonprotective antibodies on host defense is unknown. In this study we used mixtures of protective and nonprotective monoclonal antibodies (mAbs) to determine if nonprotective mAbs blocked the activity of the protective mAbs. Antibody isotype and epitope specificity are important in determining the ability to prolong survival in mice given a lethal C. neoformans infection. Three different nonprotective immunoglobulin (Ig) G23 mAbs to cryptococcal capsular polysaccharide were used to study the interaction between the IgG3 isotype and protective IgG1 and IgG2a mAbs in murine cryptococcal infection. One IgG3 mAb reduced the protective efficacy of an IgG1 with identical epitope specificity. A second IgG3 mAb with different epitope specificity also reduced the protection provided by the IgG1 mAb. The protective efficacy of an IgG2a mAb was also dramatically decreased by still another IgG3 mAb. To our knowledge this is the first report of blocking antibodies to a fungal pathogen. The results have important implications for the development of vaccines and passive antibody therapy against C. neoformans.
接种疫苗和感染可在小鼠体内引发针对新型隐球菌的保护性和非保护性抗体。非保护性抗体对宿主防御的影响尚不清楚。在本研究中,我们使用保护性和非保护性单克隆抗体(mAb)混合物来确定非保护性mAb是否会阻断保护性mAb的活性。抗体同种型和表位特异性对于确定在接受致死性新型隐球菌感染的小鼠中延长存活时间的能力很重要。使用三种针对隐球菌荚膜多糖的不同非保护性免疫球蛋白(Ig)G23 mAb来研究IgG3同种型与保护性IgG1和IgG2a mAb在小鼠隐球菌感染中的相互作用。一种IgG3 mAb降低了具有相同表位特异性的IgG1的保护效力。另一种具有不同表位特异性的IgG3 mAb也降低了IgG1 mAb提供的保护作用。还有一种IgG3 mAb也显著降低了IgG2a mAb的保护效力。据我们所知,这是关于针对真菌病原体的阻断抗体的首次报道。这些结果对开发针对新型隐球菌的疫苗和被动抗体疗法具有重要意义。