Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 1979 Oct;26(1):217-24.
doi: 10.1128/iai.26.1.217-224.1979.

Cell-mediated immunity to cytomegalovirus in immunocompromised patients: effect of radiation or chemotherapy

Cell-mediated immunity to cytomegalovirus in immunocompromised patients: effect of radiation or chemotherapy

Y Agatsuma et al. Infect Immun. 1979 Oct.

Abstract

Using the techniques of complement fixation, immunofluorescence, and in vitro lymphocyte transformation (LTF), we studied the humoral antibody and cell-mediated immunity to cytomegalovirus (CMV) in normal subjects, in patients with cancer receiving localized or nonlocalized radiation, and in renal transplant recipients on immunosuppressive chemotherapy. The LTF activity was determined by the whole blood microassay, using four strains of CMV (AD-169, Davis, Veca, and Towne), AD-169 early antigen, and phytohemagglutinin (PAH). The renal transplant subjects manifested significantly depressed LTF responses to PHA and CMV and frequent presence of immunoglobulin M and early antigen-specific antibody response. The depressed LTF response to CMV recovered significantly 2 years after transplantation. The cancer patients were also characterized by a profound drop in LTF responses to PHA and CMV and in immunoglobulin M and early antigen-specific antibody response after nonlocalized radiation. LTF responses to AD-169 and Towne strains were found to be higher than those to Davis and Veca strains. The LTF response to PHA declined with age. However, LTF responses to specific CMV antigens were found to be somewhat increased with advancing age. These observations suggest that transplantation-associated suppression of CMV-specific cell-mediated immunity may improve a few years after transplantation despite continued immunosuppressive therapy.

PubMed Disclaimer

Similar articles

Cited by

References

    1. Infect Immun. 1978 Apr;20(1):82-7 - PubMed
    1. J Clin Microbiol. 1975 Mar;1(3):262-7 - PubMed
    1. J Infect Dis. 1975 Oct;132(4):421-33 - PubMed
    1. J Infect Dis. 1976 Apr;133(4):399-408 - PubMed
    1. Am J Med. 1976 Sep;61(3):326-32 - PubMed

Publication types

Substances

LinkOut - more resources