Immunity to infection
Passive immunization with monoclonal antibody against a 70-kDa putative adhesin of Sporothrix schenckii induces protection in murine sporotrichosis
Article first published online: 7 NOV 2008
DOI: 10.1002/eji.200838513
Copyright © 2008 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim
Additional Information
How to Cite
Nascimento, R. C., Espíndola, N. M., Castro, R. A., Teixeira, P. A. C., Loureiro y Penha, C. V., Lopes-Bezerra, L. M. and Almeida, S. R. (2008), Passive immunization with monoclonal antibody against a 70-kDa putative adhesin of Sporothrix schenckii induces protection in murine sporotrichosis. Eur. J. Immunol., 38: 3080–3089. doi: 10.1002/eji.200838513
Publication History
- Issue published online: 7 NOV 2008
- Article first published online: 7 NOV 2008
- Manuscript Accepted: 26 AUG 2008
- Manuscript Revised: 25 JUL 2008
- Manuscript Received: 15 MAY 2008
Funded by
- Fundação de Amparo a Pesquisa do Estado de São Paulo. Grant Number: (FAPESP Process: 06/50472-2)
- CNPq (Conselho Nacional de Desenvolvimento Cientifico e Tecnológico
- Abstract
- Article
- References
- Cited By
Keywords:
- Adhesins;
- Mab;
- Passive immunization;
- Sporothrix schenckii;
- Sporotrichosis
Abstract
Cell-mediated and innate immunity are considered the most important mechanisms of host defense against fungus infections. However, recent studies demonstrated that specific antibodies show different degrees of protection against mycosis. In a previous study, antigens secreted by Sporothrix schenckii induced a specific humoral response in infected animals, mainly against the 70-kDa molecule, indicating a possible participation of antibodies to this antigen in infection control. In the present study, an IgG1 mAb was produced against a 70-kDa glycoprotein of S. schenckii in order to better understand the effect of passive immunization of mice infected with S. schenckii. Results showed a significant reduction in the number of CFU in organs of mice when the mAb was injected before and during S. schenckii infection. Similar results were observed when T-cell-deficient mice were used. Moreover, in a second schedule treatment, the mAb was injected after infection was established, and again we observed a significant reduction in CFU associated with an increase of IFN-γproduction. Also, the 70-kDa antigen is shown to be a putative adhesin present on the surface of this fungus. In conclusion, we report for the first time the protective effect of a specific antibody against S. schenckii.

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