Characterization of a Murine Monoclonal Antibody to Cryptococcus neoformans Polysaccharide That Is a Candidate for Human Therapeutic Studies

Author:

Casadevall Arturo12,Cleare Wendy2,Feldmesser Marta1,Glatman-Freedman Aharona3,Goldman David L.3,Kozel Thomas R.4,Lendvai Nikoletta2,Mukherjee Jean1,Pirofski Liise-anne12,Rivera Johanna2,Rosas Angel L.2,Scharff Matthew D.5,Valadon Philippe5,Westin Katherine1,Zhong Zhaojing1

Affiliation:

1. Division of Infectious Diseases, Department of Medicine,1 and Departments of

2. Microbiology and Immunology,2

3. Pediatrics,3 and

4. Department of Microbiology, School of Medicine, University of Nevada, Reno, Nevada4

5. Cell Biology,5 Albert Einstein College of Medicine, Bronx, New York, and

Abstract

ABSTRACT The murine monoclonal antibody (MAb) 18B7 [immunoglobulin G1(κ)] 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.

Publisher

American Society for Microbiology

Subject

Infectious Diseases,Pharmacology (medical),Pharmacology

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