A human IgM monoclonal antibody prolongs survival of mice with lethal cryptococcosis

Fleuridor, R.;Zhong, Z. J.;Pirofski, L. A.

Author address: 

Pirofski, LA, Yeshiva Univ Albert Einstein Coll Med, Div Infect Dis, Dept Med, Room 402 Forchheimer Bldg,1300 Morris Pk Ave, Bronx, NY 10461 USA


Antifungal therapy cannot eradicate Cryptococcus neoformans infections in immunosuppressed patient groups. Therefore, adjunctive antibody-based therapy is being considered to enhance host immune responses to C. neoformans. To characterize potentially protective reagents, the idiotypic repertoire of human antibodies to cryptococcal glucuronoxylomannan (GXM) elicited by the investigational conjugate vaccine GXM-tetanus toroid was examined. The variable genes used by human antibodies to GXM were analyzed with an antigen-based ELISA and mouse monoclonal antibodies (MAbs) that recognize determinants of human V(H)1, V(H)3, and V(H)4 gene segments. Antibodies to GXM were shown to use V(H)3 gene segments, and antibodies with the greatest binding to GXM also bound to protein A. A V(H)3- positive human monoclonal IgM prolonged survival of C. neoformans-infected mice. This is the first report that a human antibody is protective against C. neoformans. These results suggest that human MAbs may have promise as therapeutic reagents against cryptococcosis.

abstract No: 


Full conference title: 

98th Meeting of the American-Society-for-Microbiology
    • ASM 98th (1998)