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T B TOMASI

Publications and source records attributed to T B TOMASI.

15 recordsLinked to original sources

CHARACTERISTICS OF AN IMMUNE SYSTEM COMMON TO CERTAIN EXTERNAL SECRETIONS.

The gamma(1)A present in saliva and colostrum exists largely in the form of higher polymers, the major component of which has a sedimentation coefficient of 11S. The 11S gamma(1)A in these fluids differs from the polymers found in normal and myeloma sera both immunologically and by the fact that their sedimentation coefficients are unaffected by disulfide bond reduction in the absence of urea. However, like other gamma-globulins the 11S gamma(1)A molecules consist of multiple polypeptide chains linked by disulfide bonds. Local synthesis of gamma(1)A in the salivary gland has been shown by fluorescent and autoradiographic studies, although the fraction of the total salivary gamma(1)A which is derived from local production is uncertain. No evidence of transport of intravenously administered I(131)-labeled 7S gamma(1)A from serum to saliva was obtained. Immunological specificity has been demonstrated in the salivary and colostral gamma(1)A. Whether that portion of the gamma(1)A which is immunologically specific is a piece incorporated during the local synthesis of gamma(1)A in the gland or is added by the epithelial cell in the process of transport remains to be determined. Antibody activity (isohemagglutinins) have been demonstrated in saliva and colostrum and have been shown to be of the gamma(1)A-type. In both of these fluids activity is associated primarily with gamma(1)A-polymers of 11S and 18S sizes. There appears to be an immunological system which is characteristic of certain external secretions. Its properties including the local production of a distinctive type of antibody separate it from the "systemic" system responsible for the production of circulating antibody. This system may play a significant role in the body's defense mechanisms against allergens and microorganisms.

Animals↗

ACTIVITY OF DISSOCIATED AND REASSOCIATED 19S ANTI-GAMMA-GLOBULINS.

19S anti-gamma-globulins were isolated in a high state of purity from the sera of two patients with rheumatoid arthritis. Following reduction with ethyl mercaptan and alkylation by iodoacetamide, fragments were produced which retained the capacity to combine with 7S gamma-globulin. The fragments from one of the 19S anti-gamma-globulins agglutinated red cells coated with incomplete anti-Rh antibodies. This activity was shown by density gradient ultracentrifugation to be associated with low molecular weight fractions. The agglutination of the coated red cells by the fragments was strongly inhibited by normal and myeloma 7S gamma-globulins and showed a greater specificity than the parent 19S material. Analytical ultracentrifuge experiments demonstrated that the fragments from either of the 19S anti-gamma-globulins formed complexes with 7S gamma-globulin. Reassociation of the dissociated fragments through reformation of disulfide bonds resulted in the formation of fast sedimenting molecules having properties similar to those of the untreated 19S material in respect to precipitation with aggregated gamma-globulin and agglutination of coated red cells.

Antibodies, Anti-Idiotypic↗

GAMMA-GLOBULINS: QUANTITATIVE RELATIONSHIPS IN HUMAN SERUM AND NONVASCULAR FLUIDS.

Three types of gamma-globulins, gamma(2), gamma(IA), and yim, are present in certain body fluids and secretions in proportions significantly different from those of normal human serum. A lthough ylA-globulin is present in only small amounts in serum, it represents a major fraction of the gamma globulin of tears, bile, saliva, colostrum, and fluid of the small intestine.

Amniotic Fluid↗