Abstract
A reverse hemolytic plaque-forming cell (PFC) assay for the enumeration of immunoglobulin-(Ig)secreting cells in nonimmunized rabbits was developed by using erythrocytes coated with anti-Ig antibody. These indicator cells lysed after reacting with the secreted Ig antigen and complement. The anti-Ig antibodies used were specific for the b4 or b5 allotypic specificities, which are antigenic determinants on the kappa chain of rabbit Ig and controlled by alleles at the b locus. We coated erythrocytes with anti-b4 or anti-b5 antibody, using hybrid antibody with dual specificity to sheep red blood cells and to the b4 or b5 kappa chain. The coated erythrocytes were plated with cells from various lymphoid organs of nonimmunized rabbits. These lymphoid cells formed allotype-specific plaques, i.e., the cells of b4 homozygous rabbits formed hemolytic plaques with anti-b4 but not with anti-b5-coated erythrocytes and vice versa. In eight nonimmunized rabbits, 0.06-0.3% of the spleen cells (590-2900 PFC per 106 cells) secreted the b locus Ig allotypes. In three nonimmunized rabbits, 320-590 PFC per 106 cells were counted in the lymph node or bone marrow; 26-40 PFC per 106 cells were detected in the thymus. Since the b4 and b5 specificities are present on approximately 90% of the serum Ig, our results indicate that less than 1% of the lymphoid cells in nonimmunized rabbits secrete Ig at any one time. By this reverse PFC assay, Ig-secreting cells were for the first time detected as antigen-secreting cells. This assay can be applied to the detection of cells secreting other antigens.
Keywords: lymphoid organs, light chain allotypes, rosette-forming cells, antigen-reactive erythrocytes
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- Axén R., Ernback S. Chemical fixation of enzymes to cyanogen halide activated polysaccharide carriers. Eur J Biochem. 1971 Feb 1;18(3):351–360. doi: 10.1111/j.1432-1033.1971.tb01250.x. [DOI] [PubMed] [Google Scholar]
- DRAY S., YOUNG G. O., GERALD L. IMMUNOCHEMICAL IDENTIFICATION AND GENETICS OF RABBIT GAMMA-GLOBULIN ALLOTYPES. J Immunol. 1963 Sep;91:403–415. [PubMed] [Google Scholar]
- Davie J. M., Paul W. E., Mage R. G., Goldman M. B. Membrane-associated immunoglobulin of rabbit peripheral blood lymphocytes: allelic exclusion at the b locus. Proc Natl Acad Sci U S A. 1971 Feb;68(2):430–434. doi: 10.1073/pnas.68.2.430. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Dresser D. W., Wortis D. H. Use of an antiglobulin serum to detect cells producing antibody with low haemolytic efficiency. Nature. 1965 Nov 27;208(5013):859–861. doi: 10.1038/208859a0. [DOI] [PubMed] [Google Scholar]
- Golub E. S., Mishell R. I., Weigle W. O., Dutton R. W. A modification of the hemolytic plaque assay for use with protein antigens. J Immunol. 1968 Jan;100(1):133–137. [PubMed] [Google Scholar]
- HELMREICH E., KERN M., EISEN H. N. Observations on the mechanism of secretion of gamma-globulins by isolated lymph node cells. J Biol Chem. 1962 Jun;237:1925–1931. [PubMed] [Google Scholar]
- Hong R., Nisonoff A. Relative labilities of the two types of interchain disulfide bond of rabbit gamma G-immunoglobulin. J Biol Chem. 1965 Oct;240(10):3883–3891. [PubMed] [Google Scholar]
- Inman J. K., Merchant B., Claflin L., Tacey S. E. Coupling of large haptens to proteins and cell surfaces: preparation of stable, optimally sensitized erythrocytes for hapten-specific, hemolytic plaque assays. Immunochemistry. 1973 Mar;10(3):165–174. doi: 10.1016/0019-2791(73)90005-0. [DOI] [PubMed] [Google Scholar]
- NISONOFF A., PALMER J. L. HYBRIDIZATION OF HALF MOLECULES OF RABBIT GAMMA GLOBULIN. Science. 1964 Jan 24;143(3604):376–379. doi: 10.1126/science.143.3604.376. [DOI] [PubMed] [Google Scholar]
- Paraskevas F., Lee S. T., Israels L. G. Cell surface associated gamma globulins in lymphocytes. I. Reverse immune cytoadherence: a technique for their detection in mouse and human lymphocytes. J Immunol. 1971 Jan;106(1):160–170. [PubMed] [Google Scholar]
- Pasanen V. J., Mäkelä O. Effect of the number of haptens coupled to each erythrocyte on haemolytic plaque formation. Immunology. 1969 Mar;16(3):399–407. [PMC free article] [PubMed] [Google Scholar]
- Rouquès R., Inman J. K., Merchant B. Detection of cells secreting antibodies more reactive with an alternate structure than with the immunizing hapten. Int Arch Allergy Appl Immunol. 1972;42(6):852–870. doi: 10.1159/000230663. [DOI] [PubMed] [Google Scholar]
- Sterzl J., Ríha I. Detection of cells producing 7S antibodies by the plaque technique. Nature. 1965 Nov 27;208(5013):858–859. doi: 10.1038/208858a0. [DOI] [PubMed] [Google Scholar]
- Sweet G. H., Welborn F. L. Use of chromium chloride as the coupling agent in a modified plaque assay. Cells producing anti-protein antibody. J Immunol. 1971 May;106(5):1407–1410. [PubMed] [Google Scholar]
- Wolf B., Janeway C. A., Jr, Coombs R. R., Catty D., Gell P. G., Kelus A. S. Immunoglobulin determinants on the lymphocytes of normal rabbits. 3. As4 and As6 determinants on individual lymphocytes and the concept of allelic exclusion. Immunology. 1971 Jun;20(6):931–944. [PMC free article] [PubMed] [Google Scholar]

