AGE-DEPENDENT VARIATIONS OF ANTIBODY AVIDITY
- 1 January 1978
- journal article
- research article
- Vol. 35 (4), 601-611
Abstract
Age-dependent variations of antibody avidity were sutdied in the C3HeB/FeJ mouse. Spleen cells from donors of different ages (10-720 days) were transferred and stimulated with TNP-HRBC [trinitrophenylaed horse erythrocytes] in lethally irradiated syngenic recipients. The anti-TNP antibody response of the donor cells was estimated from the number of direct PFC [plaque forming cells] per recipient spleen by the Jerne technique with TNP-S[sheep]RBC. Avidity of the antibodies secreted by PFC was evaluated from the amount of added TNP-BSA [bovine serum albumin] that inhibited 50% of the anti-TNP PFC. Under these experimental conditions allowing the exclusion of any influence of the donor milieu during the immune response, age-dependent variations of the antibody response and avidity could be attributed to changes in the donor spleen cell population. Avidity increased with the response and varied parabolically with age. After appropriate correction of the number of PFC to make it independent from age, avidity values were fitted by a multiple curvilinear regression in which the independent variables playing a significant role were the corrected number of PFC in its linear term and the age in its linear and quadratic terms. From comparison of the standard coefficients of this regression, the observed variations of avidity could be attributed in part (82%) to the response and inpart (18%) to the age. For any value of response, avidity increased 15-fold from day 10 to reach a maximum at day 110 and then declined 5-fold at the age of 720 days. Heterogeneity of avidity also changed parabolically with age as high avidity classes were present in adulthood and absent at 10 and 720 days.This publication has 61 references indexed in Scilit:
- B-lymphocyte heterogeneity: ontogenetic development and organ distribution of B-lymphocyte populations defined by their density of surface immunoglobulin.The Journal of Experimental Medicine, 1976
- Measurement and comparison of the proliferative and antibody responses of neonatal, immature and adult murine spleen cells to T-dependent and T-independent antigensCellular Immunology, 1976
- Suppression of the immune response by alpha-fetoprotein on the primary and secondary antibody response.The Journal of Experimental Medicine, 1975
- Ontogeny of mouse lymphocyte function. II. Development of the ability to produce antibody is modulated by T lymphocytes.The Journal of Experimental Medicine, 1975
- Cell surface immunoglobulin. XI. The appearance of an IgD-like molecule on murine lymphoid cells during ontogeny.The Journal of Experimental Medicine, 1975
- SELECTIVE ROLES OF THYMUS-DERIVED LYMPHOCYTES IN THE ANTIBODY RESPONSEThe Journal of Experimental Medicine, 1974
- Repetition of molecular-genetic information as a possible factor in evolutionary changes of life spanExperimental Gerontology, 1972
- THE MECHANISM OF ANTIGENIC STIMULATION OF PRIMARY AND SECONDARY CLONAL PRECURSOR CELLSThe Journal of Experimental Medicine, 1972
- Codon-restriction theory of aging and developmentJournal of Theoretical Biology, 1971
- Plaque Formation in Agar by Single Antibody-Producing CellsScience, 1963