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Immunohistologic analysis of a human pulmonary alveolar macrophage antigen

dc.contributor.authorKobzik, Lesteren_US
dc.contributor.authorGodleski, John J.en_US
dc.contributor.authorBiondi, Andreaen_US
dc.contributor.authorO'Hara, Carl J.en_US
dc.contributor.authorTodd, Robert F. IIIen_US
dc.date.accessioned2006-04-07T18:55:01Z
dc.date.available2006-04-07T18:55:01Z
dc.date.issued1985-11en_US
dc.identifier.citationKobzik, Lester, Godleski, John J., Biondi, Andrea, O'Hara, Carl J., Todd, III, Robert F. (1985/11)."Immunohistologic analysis of a human pulmonary alveolar macrophage antigen." Clinical Immunology and Immunopathology 37(2): 213-219. <http://hdl.handle.net/2027.42/25512>en_US
dc.identifier.urihttp://www.sciencedirect.com/science/article/B6WCK-4C4NX4H-D6/2/47723c2b71d7c6492f83360a4af3faaeen_US
dc.identifier.urihttps://hdl.handle.net/2027.42/25512
dc.identifier.urihttp://www.ncbi.nlm.nih.gov/sites/entrez?cmd=retrieve&db=pubmed&list_uids=3899433&dopt=citationen_US
dc.description.abstractPAM1 is a 200-kDa polypeptide antigen present on lavaged human alveolar macrophages but not on monocytes, peritoneal macrophages, breast milk macrophages, or other normal hematopoietic cells studied by flow cytometry. We have characterized the distribution of expression of this antigen by cells in tissues by using immunohistologic techniques. Normal and diseased lung as well as lymph nodes, spleen, kidney, liver, GI tract, and skin were studied. PAM1 was expressed strongly on the surface and weakly in the cytoplasm of most alveolar macrophages in all 15 of the lung specimens. Occasional interstitial macrophages had weak to moderate staining for this antigen but the majority did not stain. The distribution, pattern, and intensity of staining for PAM1 was the same in normal lung specimens and those with interstitial pneumonitis, despite the increase in mononuclear cells in the latter. Dermal histiocytes and Kuppfer cells expressed PAM1 weakly. Sinus histiocytes in lymph nodes were moderately to strongly positive. Although lymphoid cell suspensions (tonsil) were negative by flow cytometry, five of six lymph nodes had positive cells by immunohistology. PAM1 was also detected on endothelial cells of splenic sinusoids in all 6 specimens but not on any other endothelium. Hence, while PAM1 is expressed most strongly on alveolar macrophages, it can also be demonstrated in other locations using sensitive immunohistologic techniques. Since circulating monocytes are antigen negative and some lung interstitial macrophages bear antigen, PAM1 may be a useful marker for studies of the differentiation of mononuclear cells in the lung.en_US
dc.format.extent718151 bytes
dc.format.extent3118 bytes
dc.format.mimetypeapplication/pdf
dc.format.mimetypetext/plain
dc.language.isoen_US
dc.publisherElsevieren_US
dc.titleImmunohistologic analysis of a human pulmonary alveolar macrophage antigenen_US
dc.typeArticleen_US
dc.rights.robotsIndexNoFollowen_US
dc.subject.hlbsecondlevelMicrobiology and Immunologyen_US
dc.subject.hlbsecondlevelInternal Medicine and Specialtiesen_US
dc.subject.hlbtoplevelScienceen_US
dc.subject.hlbtoplevelHealth Sciencesen_US
dc.description.peerreviewedPeer Revieweden_US
dc.contributor.affiliationumThe Department of Internal Medicine, University of Michigan Medical School, Ann Arbor, Michigan 48109, USA; Division of Tumor Immunology, Dana-Farber Cancer Institute, Boston, Massachusetts 02115, USAen_US
dc.contributor.affiliationotherDepartment of Pathology, Brigham & Women's Hospital, Boston, Massachusetts 02115, USAen_US
dc.contributor.affiliationotherDepartment of Pathology, Brigham & Women's Hospital, Boston, Massachusetts 02115, USAen_US
dc.contributor.affiliationotherDivision of Tumor Immunology, Dana-Farber Cancer Institute, Boston, Massachusetts 02115, USAen_US
dc.contributor.affiliationotherDepartment of Pathology, New England Deaconness Hospital, Boston, Massachusetts 02115, USAen_US
dc.identifier.pmid3899433en_US
dc.description.bitstreamurlhttp://deepblue.lib.umich.edu/bitstream/2027.42/25512/1/0000053.pdfen_US
dc.identifier.doihttp://dx.doi.org/10.1016/0090-1229(85)90152-7en_US
dc.identifier.sourceClinical Immunology and Immunopathologyen_US
dc.owningcollnameInterdisciplinary and Peer-Reviewed


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