Casadevall A, Cleare W, Feldmesser M, Glatman-Freedman A, Goldman D L, Kozel T R, Lendvai N, Mukherjee J, Pirofski L A, Rivera J, Rosas A L, Scharff M D, Valadon P, Westin K, Zhong Z
Department of Medicine, Albert Einstein College of Medicine, Bronx, New York 10461, USA.
Antimicrob Agents Chemother. 1998 Jun;42(6):1437-46. doi: 10.1128/AAC.42.6.1437.
The murine monoclonal antibody (MAb) 18B7 [immunoglobulin G1(kappa)] is in preclinical development for treatment of Cryptococcus neoformans infections. In anticipation of its use in humans, we defined the serological and biological properties of MAb 18B7 in detail. Structural comparison to the related protective MAb 2H1 revealed conservation of the antigen binding site despite several amino acid differences. MAb 18B7 was shown by immunofluorescence and agglutination studies to bind to all four serotypes of C. neoformans, opsonize C. neoformans serotypes A and D, enhance human and mouse effector cell antifungal activity, and activate the complement pathway leading to deposition of complement component 3 (C3) on the cryptococcal capsule. Administration of MAb 18B7 to mice led to rapid clearance of serum cryptococcal antigen and deposition in the liver and spleen. Immunohistochemical studies revealed that MAb 18B7 bound to capsular glucuronoxylomannan in infected mouse tissues. No reactivity of MAb 18B7 with normal human, rat, or mouse tissues was detected. The results show that both the variable and constant regions of MAb 18B7 are biologically functional and support the use of this MAb in human therapeutic trials.
鼠单克隆抗体(MAb)18B7[免疫球蛋白G1(κ)]正处于治疗新型隐球菌感染的临床前开发阶段。为了预期其在人类中的应用,我们详细定义了MAb 18B7的血清学和生物学特性。与相关保护性单克隆抗体2H1的结构比较显示,尽管存在几个氨基酸差异,但抗原结合位点保持保守。免疫荧光和凝集研究表明,MAb 18B7可与新型隐球菌的所有四种血清型结合,调理新型隐球菌血清型A和D,增强人和小鼠效应细胞的抗真菌活性,并激活补体途径,导致补体成分3(C3)沉积在隐球菌荚膜上。给小鼠注射MAb 18B7可导致血清隐球菌抗原迅速清除并沉积在肝脏和脾脏中。免疫组织化学研究表明,MAb 18B7与感染小鼠组织中的荚膜葡糖醛酸木聚糖结合。未检测到MAb 18B7与正常人、大鼠或小鼠组织的反应性。结果表明,MAb 18B7的可变区和恒定区均具有生物学功能,并支持该单克隆抗体用于人类治疗试验。