Literature DB >> 6798127

Tissue origins of human polymeric and monomeric IgA.

W H Kutteh, S J Prince, J Mestecky.   

Abstract

Human tissues were examined for their ability to produce monomeric and polymeric forms of IgA in vitro. Mononuclear cells were examined for the presence of cytoplasmic immunoglobulins and J chain (by immunofluorescence) and for the amounts and molecular forms of intracellular and secreted IgA (by radioimmunoassay). Cultured bone marrow cells were the largest producers of total IgA, and approximately 90% of the secreted IgA was monomeric. Spleen cells also produced predominantly monomeric IgA. Intestinal lamina propria cells secreted the greatest amounts of polymeric IgA, but also produced significant amounts of monomeric IgA. Tonsillar, lymph node, and peripheral blood cells produced approximately equal proportions of monomeric and polymeric IgA. These results suggested that bone marrow may be a major source of serum monomeric IgA, and that lymphoid tissues associated with secretory surfaces may provide a greater proportion of polymeric IgA than other lymphoid tissues. There was a positive correlation between the production of polymeric IgA and the presence of cytoplasmic J chain; tissues that produced predominantly monomeric IgA generally displayed fewer cells containing cytoplasmic J chain.

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Year:  1982        PMID: 6798127

Source DB:  PubMed          Journal:  J Immunol        ISSN: 0022-1767            Impact factor:   5.422


  52 in total

Review 1.  Dysfunctions of the Iga system: a common link between intestinal and renal diseases.

Authors:  Christina Papista; Laureline Berthelot; Renato C Monteiro
Journal:  Cell Mol Immunol       Date:  2011-01-31       Impact factor: 11.530

Review 2.  The structure and function of human IgA.

Authors:  M A Kerr
Journal:  Biochem J       Date:  1990-10-15       Impact factor: 3.857

3.  Jejunal immunoglobulin and antigliadin antibody secretion in adult coeliac disease.

Authors:  J F Colombel; F Mascart-Lemone; J Nemeth; J P Vaerman; C Dive; J C Rambaud
Journal:  Gut       Date:  1990-12       Impact factor: 23.059

4.  Increased and prolonged production of specific polymeric IgA after systemic immunization with tetanus toxoid in IgA nephropathy.

Authors:  L Layward; A C Allen; S J Harper; J M Hattersley; J Feehally
Journal:  Clin Exp Immunol       Date:  1992-06       Impact factor: 4.330

5.  Enumeration of IgA producing cells by the enzyme linked immunospot (ELISPOT) technique to evaluate sulphasalazine effects in inflammatory arthritides.

Authors:  N Feltelius; S Gudmundsson; L Wennersten; O Sjöberg; R Hällgren; L Klareskog
Journal:  Ann Rheum Dis       Date:  1991-06       Impact factor: 19.103

6.  Cellular origins of human polymeric and monomeric IgA: enumeration of single cells secreting polymeric IgA1 and IgA2 in peripheral blood, bone marrow, spleen, gingiva and synovial tissue.

Authors:  A Tarkowski; Z Moldoveanu; W J Koopman; J Radl; J J Haaijman; J Mestecky
Journal:  Clin Exp Immunol       Date:  1991-08       Impact factor: 4.330

7.  [Alcohol and IgA in the kidney].

Authors:  H Köhler
Journal:  Klin Wochenschr       Date:  1985-09-16

8.  Intraperitoneal immunization of human subjects with tetanus toxoid induces specific antibody-secreting cells in the peritoneal cavity and in the circulation, but fails to elicit a secretory IgA response.

Authors:  C Lue; A W van den Wall Bake; S J Prince; B A Julian; M L Tseng; J Radl; C O Elson; J Mestecky
Journal:  Clin Exp Immunol       Date:  1994-05       Impact factor: 4.330

9.  Kinetics of anti-Campylobacter jejuni monomeric and polymeric immunoglobulin A1 and A2 responses in serum during acute enteritis.

Authors:  F O Mascart-Lemone; J R Duchateau; J Oosterom; J P Butzler; D L Delacroix
Journal:  J Clin Microbiol       Date:  1987-07       Impact factor: 5.948

10.  Significance of different J chain profiles in human tissues: generation of IgA and IgM with binding site for secretory component is related to the J chain expressing capacity of the total local immunocyte population, including IgG and IgD producing cells, and depends on the clinical state of the tissue.

Authors:  P Brandtzaeg; F R Korsrud
Journal:  Clin Exp Immunol       Date:  1984-12       Impact factor: 4.330

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