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Comparison of the cellular cytotoxic activities of colostral lymphocytes and maternal peripheral blood lymphocytes

dc.contributor.authorNair, Madhavan P. N.en_US
dc.contributor.authorSchwartz, Stanley A.en_US
dc.contributor.authorSlade, Herbert B.en_US
dc.contributor.authorJohnson, Mary Z.en_US
dc.contributor.authorQuebbeman, James F.en_US
dc.contributor.authorBeer, Alan E.en_US
dc.date.accessioned2006-04-07T19:05:11Z
dc.date.available2006-04-07T19:05:11Z
dc.date.issued1985-05en_US
dc.identifier.citationNair, Madhavan P. N., Schwartz, Stanley A., Slade, Herbert B., Johnson, Mary Z., Quebbeman, James F., Beer, Alan E. (1985/05)."Comparison of the cellular cytotoxic activities of colostral lymphocytes and maternal peripheral blood lymphocytes." Journal of Reproductive Immunology 7(3): 199-213. <http://hdl.handle.net/2027.42/25675>en_US
dc.identifier.urihttp://www.sciencedirect.com/science/article/B6T8W-476VS35-3T/2/bf542d758a1bc430eedf82893c4e71aden_US
dc.identifier.urihttps://hdl.handle.net/2027.42/25675
dc.identifier.urihttp://www.ncbi.nlm.nih.gov/sites/entrez?cmd=retrieve&db=pubmed&list_uids=2410614&dopt=citationen_US
dc.description.abstractColostral lymphocytes (CL) from mothers 2 to 4 days post-partum and autologous maternal peripheral blood lymphocytes (PBL) were investigated for (1) natural killer (NK) and antibody-dependent cellular cytotoxic (ADCC) activities, (2) target binding ability, (3) interferon (IFN)- and interleukin 2 (IL2)-induced augmentation of NK activity, (4) lectin-dependent cellular cytotoxicity (LDCC), and (5) the ability of culture-derived soluble suppressor factor(s) to inhibit the NK activity of normal allogeneic lymphocytes. CL depleted of adherent cells and Percoll-separated NK-enriched subpopulations of CL demonstrated significantly lower NK and ADCC activities compared to autologous PBL. However, the target binding ability of CL was comparable to autologous PBL. Although the residual NK activity of CL was augmented by IFN and IL2, the activity was not enhanced to the same level shown by autologous PBL. CL also demonstrated a significant enhancement of LDCC activity, although the activity was not stimulated to the levels shown by PBL. Culture supernates of CL manifested greater suppression of the NK ability of allogeneic PBL than culture supernates produced by autologous PBL. These results are consistent with a model that suggests differential partitioning of lymphocyte subpopulations between colostrum and peripheral blood.en_US
dc.format.extent896817 bytes
dc.format.extent3118 bytes
dc.format.mimetypeapplication/pdf
dc.format.mimetypetext/plain
dc.language.isoen_US
dc.publisherElsevieren_US
dc.titleComparison of the cellular cytotoxic activities of colostral lymphocytes and maternal peripheral blood lymphocytesen_US
dc.typeArticleen_US
dc.rights.robotsIndexNoFollowen_US
dc.subject.hlbsecondlevelPublic Healthen_US
dc.subject.hlbsecondlevelObstetrics and Gynecologyen_US
dc.subject.hlbsecondlevelInternal Medicine and Specialtiesen_US
dc.subject.hlbtoplevelHealth Sciencesen_US
dc.description.peerreviewedPeer Revieweden_US
dc.contributor.affiliationumDepartment of Pediatrics, University of Michigan, Ann Arbor, MI 48109, U.S.A.; Department of Epidemiology, University of Michigan, Ann Arbor, MI 48109, U.S.A.en_US
dc.contributor.affiliationumDepartment of Pediatrics, University of Michigan, Ann Arbor, MI 48109, U.S.A.; Department of Epidemiology, University of Michigan, Ann Arbor, MI 48109, U.S.A.en_US
dc.contributor.affiliationumDepartment of Pediatrics, University of Michigan, Ann Arbor, MI 48109, U.S.A.en_US
dc.contributor.affiliationumDepartment of Obstetrics and Gynecology, University of Michigan, Ann Arbor, MI 48109, U.S.A.en_US
dc.contributor.affiliationumDepartment of Obstetrics and Gynecology, University of Michigan, Ann Arbor, MI 48109, U.S.A.en_US
dc.contributor.affiliationumDepartment of Obstetrics and Gynecology, University of Michigan, Ann Arbor, MI 48109, U.S.A.en_US
dc.identifier.pmid2410614en_US
dc.description.bitstreamurlhttp://deepblue.lib.umich.edu/bitstream/2027.42/25675/1/0000228.pdfen_US
dc.identifier.doihttp://dx.doi.org/10.1016/0165-0378(85)90051-8en_US
dc.identifier.sourceJournal of Reproductive Immunologyen_US
dc.owningcollnameInterdisciplinary and Peer-Reviewed


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