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


     
 


The Journal of Immunology, 1973, 111: 1101-1107.
Copyright © 1973 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 Hallgren, H. M.
Right arrow Articles by Yunis, E. J.
Right arrow Search for Related Content
PubMed
Right arrow Articles by Hallgren, H. M.
Right arrow Articles by Yunis, E. J.

Lymphocyte Phytohemagglutinin Responsiveness, Immunoglobulins and Autoantibodies in Aging Humans1

H. M. Hallgren, C. E. Buckley, III, V. A. Gilbertsen and E. J. Yunis

From the Departments of Laboratory Medicine and Surgery, University of Minnesota, Minneapolis, Minnesota, and the Departments of Medicine and Microbiology-Immunology and the Center for Study of Human Development and Aging, Duke University Medical Center, Durham, North Carolina

Abstract

Phytohemagglutinin responsiveness of peripheral blood lymphocytes declines in aged humans. Older humans exhibit a rise in the incidence of autoantibodies. The incidence of autoantibodies becomes significantly greater among older subjects over 80 years of age and is most significant in humans with low lymphocyte phytohemagglutinin responses. Serum levels of IgG and IgA were increased in subjects surviving beyond the 7th decade. Correlations could not be detected between serum immunoglobulin levels, titers of individual autoantibodies and the lymphocyte response to phytohemagglutinin. These observations suggest that hyperglobulinemia, impaired lymphocyte phytohemagglutinin responsiveness, and increased frequency of autoantibodies are characteristic of surviving older humans and represent associated events in the natural history of human life.

Footnotes

1 This work was supported by United States Public Health Service Grants HD 00668, AI 10153 and HL 06314 from the National Institutes of Health, Bethesda, Maryland, and funds from the Department of Laboratory Medicine, University of Minnesota.




This article has been cited by other articles:


Home page
LupusHome page
M Ramos-Casals, M Garcia-Carrasco, M P Brito, A Lopez-Soto, and J Font
Autoimmunity and geriatrics: clinical significance of autoimmune manifestations in the elderly
Lupus, May 1, 2003; 12(5): 341 - 355.
[Abstract] [PDF]


Home page
Arch Intern MedHome page
P. J. Carson, K. L. Nichol, J. O'Brien, P. Hilo, and E. N. Janoff
Immune Function and Vaccine Responses in Healthy Advanced Elderly Patients
Arch Intern Med, July 10, 2000; 160(13): 2017 - 2024.
[Abstract] [Full Text] [PDF]


Home page
Int ImmunolHome page
A. S. Eaton-Bassiri, L. Mandik-Nayak, S.-j. Seo, M. P. Madaio, M. P. Cancro, and J. Erikson
Alterations in splenic architecture and the localization of anti-double-stranded DNA B cells in aged mice
Int. Immunol., June 1, 2000; 12(6): 915 - 926.
[Abstract] [Full Text] [PDF]


Home page
ThoraxHome page
K. C Meyer and P. Soergel
Variation of bronchoalveolar lymphocyte phenotypes with age in the physiologically normal human lung
Thorax, August 1, 1999; 54(8): 697 - 700.
[Abstract] [Full Text]




HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
This Website Copyright © 1973 by The American Association of Immunologists, Inc. All rights reserved.
All Contents Copyright © 1973 by The American Association of Immunologists, Inc. All rights reserved.