The JI
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
 QUICK SEARCH:   [advanced]


     
 


The Journal of Immunology, 1968, 100: 569-580.
Copyright © 1968 by The American Association of Immunologists, Inc.

This Article
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 Alert me to new issues of the journal
Right arrow Download to citation manager
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Westaway, E. G.
Right arrow Search for Related Content
PubMed
Right arrow Articles by Westaway, E. G.

Antibody Responses in Rabbits to the Group B Arbovirus Kunjin: Serologic Activity of the Fractionated Immunoglobulins in Homologous and Heterologous Reactions

E. G. Westaway1,2,

From the Yale Arbovirus Research Unit, Yale University School of Medicine, New Haven, Connecticut, and The Queensland Institute of Medical Research, Herston, Brisbane, Australia

Abstract

IgM, electrophoretically fast IgG and slow IgG fractions of rabbit {gamma}-globulin were separated using DEAE-cellulose columns, gel filtration and/or ultracentrifugation. The early appearance of IgM and fast IgG antibodies and the later appearance of slow IgG antibodies were correlated in hemagglutination-inhibition (HI) tests and in plaque reduction neutralization tests (NT). All fractions from 7-day immune serum were potentiated in NT by fresh normal serum, but the effect declined markedly during immunization. IgM and IgG fractions were potentiated by the addition of anti-rabbit {gamma}-globulin to NT mixtures. Dose-response experiments revealed differences in the combining capacities of IgG fractions obtained from the same serum or at different times during immunization. A persistent fraction of approximately 10% was observed in NT with IgM antibodies.

In HI tests with other group B arboviruses, IgM and slow IgG antibodies cross-reacted less than fast IgG antibodies. Neutralizing antibodies in the fractions reacted more specifically when tested separately but synergistic activity in cross-reactions was observed when fractions were recombined. Inclusion of fresh serum in cross NT produced some loss of specificity.

The results were discussed in relation to the probable disposition of antigen-antibody complexes forming a critical area on each neutralized virus particle.

Footnotes

Supported in part by United States Public Health Service International Postdoctoral Fellowship 1 F05-TW-1045-01 from the Office of International Research, National Institutes of Health.

2 Present address: Queensland Institute of Medical Research, Herston, Brisbane, Australia.




This article has been cited by other articles:


Home page
J. Virol.Home page
W. J. Liu, X. J. Wang, V. V. Mokhonov, P.-Y. Shi, R. Randall, and A. A. Khromykh
Inhibition of Interferon Signaling by the New York 99 Strain and Kunjin Subtype of West Nile Virus Involves Blockage of STAT1 and STAT2 Activation by Nonstructural Proteins
J. Virol., February 1, 2005; 79(3): 1934 - 1942.
[Abstract] [Full Text] [PDF]


Home page
J. Biol. Chem.Home page
M. Nomaguchi, T. Teramoto, L. Yu, L. Markoff, and R. Padmanabhan
Requirements for West Nile Virus (-)- and (+)-Strand Subgenomic RNA Synthesis in Vitro by the Viral RNA-dependent RNA Polymerase Expressed in Escherichia coli
J. Biol. Chem., March 26, 2004; 279(13): 12141 - 12151.
[Abstract] [Full Text] [PDF]


Home page
Proc. Natl. Acad. Sci. USAHome page
R. A. Hall, D. J. Nisbet, K. B. Pham, A. T. Pyke, G. A. Smith, and A. A. Khromykh
DNA vaccine coding for the full-length infectious Kunjin virus RNA protects mice against the New York strain of West Nile virus
PNAS, September 2, 2003; 100(18): 10460 - 10464.
[Abstract] [Full Text] [PDF]




HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
This Website Copyright © 1968 by The American Association of Immunologists, Inc. All rights reserved.
All Contents Copyright © 1968 by The American Association of Immunologists, Inc. All rights reserved.