This Article
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrowReprints and Permissions
Right arrow Copyright Information
Right arrow Books from ASM Press
Right arrow MicrobeWorld
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Wellington, M.
Right arrow Articles by Haidaris, C. G.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Wellington, M.
Right arrow Articles by Haidaris, C. G.

 Previous Article  |  Next Article 

Infection and Immunity, December 2003, p. 7228-7231, Vol. 71, No. 12
0019-9567/03/$08.00+0     DOI: 10.1128/IAI.71.12.7228-7231.2003
Copyright © 2003, American Society for Microbiology. All Rights Reserved.

Enhanced Phagocytosis of Candida Species Mediated by Opsonization with a Recombinant Human Antibody Single-Chain Variable Fragment

Melanie Wellington,1,2 Joseph M. Bliss,1,{dagger} and Constantine G. Haidaris2,3*

Department of Pediatrics,1 Department of Microbiology and Immunology,2 Center for Oral Biology, University of Rochester School of Medicine and Dentistry, Rochester, New York 146423

Received 29 July 2003/ Returned for modification 8 August 2003/ Accepted 15 September 2003

Specific antibody opsonization significantly enhances the level of phagocytosis of Candida in the absence of complement. Furthermore, we have described a system using a recombinant human antibody single-chain variable fragment that allows a comparative study of phagocytosis of multiple Candida species opsonized via a common antigen.


* Corresponding author. Mailing address: Department of Microbiology and Immunology, University of Rochester School of Medicine and Dentistry, 601 Elmwood Ave., Box 672, Rochester, NY 14642. Phone: (585) 275-0678. Fax: (585) 473-9573. E-mail: haid{at}mail.rochester.edu.

Editor: T. R. Kozel

{dagger} Present address: Department of Pediatrics, Women and Infants' Hospital of Rhode Island, Brown University School of Medicine, Providence, RI 02905.


Infection and Immunity, December 2003, p. 7228-7231, Vol. 71, No. 12
0019-9567/03/$08.00+0     DOI: 10.1128/IAI.71.12.7228-7231.2003
Copyright © 2003, American Society for Microbiology. All Rights Reserved.




This article has been cited by other articles:

  • Rodrigo, W. W. S. I., Jin, X., Blackley, S. D., Rose, R. C., Schlesinger, J. J. (2006). Differential Enhancement of Dengue Virus Immune Complex Infectivity Mediated by Signaling-Competent and Signaling-Incompetent Human Fc{gamma}RIA (CD64) or Fc{gamma}RIIA (CD32).. J. Virol. 80: 10128-10138 [Abstract] [Full Text]  
  • Zhang, M. X., Bohlman, M. C., Itatani, C., Burton, D. R., Parren, P. W. H. I., St. Jeor, S. C., Kozel, T. R. (2006). Human Recombinant Antimannan Immunoglobulin G1 Antibody Confers Resistance to Hematogenously Disseminated Candidiasis in Mice. Infect. Immun. 74: 362-369 [Abstract] [Full Text]