Gigliotti F, Haidaris C G
University of Rochester School of Medicine & Dentistry, NY 14642, USA.
Semin Respir Infect. 1998 Dec;13(4):313-22.
Studies of Pneumocystis carinii have been limited by our inability to propagate it in continuous culture. In this context, studies of P. carinii antigens have provided significant insight into the biology of this organism. The mannose-rich surface major surface glycoprotein of P. carinii termed glycoprotein A (gpA) is the best studied of these P. carinii antigens. Significant genetic and immunologic diversity exists between the gpA molecules expressed by P. carinii derived from different mammalian sources. The molecular and biochemical nature of gpA and other P. carinii antigens including p55 are reviewed. In addition, available information concerning the role of P. carinii gpA and other antigens in host-organism interactions are also discussed.
卡氏肺孢子菌的研究一直受到我们无法在连续培养中繁殖它的限制。在此背景下,对卡氏肺孢子菌抗原的研究为深入了解这种生物体的生物学特性提供了重要线索。卡氏肺孢子菌富含甘露糖的表面主要表面糖蛋白,称为糖蛋白A(gpA),是这些卡氏肺孢子菌抗原中研究得最深入的。来自不同哺乳动物来源的卡氏肺孢子菌所表达的gpA分子之间存在显著的遗传和免疫多样性。本文综述了gpA和其他卡氏肺孢子菌抗原(包括p55)的分子和生化性质。此外,还讨论了有关卡氏肺孢子菌gpA和其他抗原在宿主 - 生物体相互作用中的作用的现有信息。