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- W2029863258 abstract "We compared the immunological functions of interferon‐γ (IFN‐γ)‐induced, classically activated macrophages (caMΦ) and of interleukin‐4 (IL‐4)‐ and glucocorticoid‐induced, alternatively activated macrophages (aaMΦ) in a human co‐culture system in vitro . Proliferation of peripheral blood leucocytes (PBL) or CD4 + T cells mediated by optimal doses of phytohaemagglutinin (PHA) or concanavalin A (Con A) was only marginally influenced by caMΦ, but was strongly inhibited by aaMΦ. The degree of lymphocyte proliferation sustained in the presence of caMΦ was gradually reduced in a dose‐dependent fashion by the addition of aaMΦ. Flow cytometric analysis revealed that expression of costimulatory molecules such as CD11a, CD40, CD54, CD58, CD80 and CD86 did not vary significantly between caMΦ and aaMΦ and was low for CD58, CD80 and CD86. As shown by reverse transcriptase‐polymerase chain reaction (RT‐PCR) analysis, IL‐10 was expressed in caMΦ, aaMΦ and control macrophages; the level of expression of IL‐10 was slightly enhanced in aaMΦ. Neither neutralizing anti‐IL‐10 antibodies, indomethacin nor N G ‐monomethyl‐l‐arginine (NMMLA) was able to reverse aaMΦ‐mediated inhibition of lymphocyte proliferation. Of several agents interfering with various second messenger pathways, cAMP and the Ca 2+ ‐ionophor A23187 inhibited differentiation of cultured human monocytes into phenotypically mature aaMΦ expressing MS‐1 high molecular weight protein (MS‐1‐HMWP) and RM 3/1 antigen, and prevented the suppressive action of aaMΦ on lymphocyte proliferation. In conclusion, these results show that aaMΦ actively inhibit mitogen‐mediated proliferation of PBL and CD4 + T cells independently of the expression of costimulatory molecules and of IL‐10, NO or prostaglandin synthesis, and that inhibition of phenotypic differentiation of aaMΦ is paralleled by a lack of functional maturation. Thus, fully matured aaMΦ may be functional in down‐regulating CD4 + T‐cell‐mediated immune reactions by an as yet unknown mechanism." @default.
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- W2029863258 date "1997-12-01" @default.
- W2029863258 modified "2023-10-18" @default.
- W2029863258 title "Alternatively activated macrophages actively inhibit proliferation of peripheral blood lymphocytes and CD4 <sup>+</sup> T cells <i>in vitro</i>" @default.
- W2029863258 cites W110518993 @default.
- W2029863258 cites W116160248 @default.
- W2029863258 cites W120940030 @default.
- W2029863258 cites W130202728 @default.
- W2029863258 cites W1527682633 @default.
- W2029863258 cites W1536939386 @default.
- W2029863258 cites W1550476728 @default.
- W2029863258 cites W1572210960 @default.
- W2029863258 cites W1580422827 @default.
- W2029863258 cites W1582931654 @default.
- W2029863258 cites W1617634120 @default.
- W2029863258 cites W1663730150 @default.
- W2029863258 cites W166691382 @default.
- W2029863258 cites W1762742043 @default.
- W2029863258 cites W1879285225 @default.
- W2029863258 cites W1907642673 @default.
- W2029863258 cites W1921414939 @default.
- W2029863258 cites W1932015869 @default.
- W2029863258 cites W1942338820 @default.
- W2029863258 cites W1963571770 @default.
- W2029863258 cites W1969327070 @default.
- W2029863258 cites W1973331834 @default.
- W2029863258 cites W1974204636 @default.
- W2029863258 cites W1974537999 @default.
- W2029863258 cites W1976865493 @default.
- W2029863258 cites W1978641660 @default.
- W2029863258 cites W1978842513 @default.
- W2029863258 cites W1979080480 @default.
- W2029863258 cites W1979572776 @default.
- W2029863258 cites W1980340532 @default.
- W2029863258 cites W1984188855 @default.
- W2029863258 cites W1984643187 @default.
- W2029863258 cites W1994095525 @default.
- W2029863258 cites W1994334214 @default.
- W2029863258 cites W2000076767 @default.
- W2029863258 cites W2003677779 @default.
- W2029863258 cites W2006048924 @default.
- W2029863258 cites W2008057379 @default.
- W2029863258 cites W2008776968 @default.
- W2029863258 cites W2014278115 @default.
- W2029863258 cites W2016015665 @default.
- W2029863258 cites W2041178171 @default.
- W2029863258 cites W2047030782 @default.
- W2029863258 cites W2049702967 @default.
- W2029863258 cites W2065361828 @default.
- W2029863258 cites W2067201373 @default.
- W2029863258 cites W2069282777 @default.
- W2029863258 cites W2069955769 @default.
- W2029863258 cites W2073589562 @default.
- W2029863258 cites W2075467451 @default.
- W2029863258 cites W2079342890 @default.
- W2029863258 cites W2086592423 @default.
- W2029863258 cites W2093260009 @default.
- W2029863258 cites W2099826413 @default.
- W2029863258 cites W2109484445 @default.
- W2029863258 cites W2120794083 @default.
- W2029863258 cites W2123640179 @default.
- W2029863258 cites W2126043069 @default.
- W2029863258 cites W2136064809 @default.
- W2029863258 cites W2141523423 @default.
- W2029863258 cites W2148619935 @default.
- W2029863258 cites W2152894118 @default.
- W2029863258 cites W2154771862 @default.
- W2029863258 cites W2159075850 @default.
- W2029863258 cites W2163526297 @default.
- W2029863258 cites W2182689213 @default.
- W2029863258 cites W2183875941 @default.
- W2029863258 cites W2186358312 @default.
- W2029863258 cites W2299322376 @default.
- W2029863258 cites W2394487098 @default.
- W2029863258 cites W2399940562 @default.
- W2029863258 cites W2401599854 @default.
- W2029863258 cites W2403444825 @default.
- W2029863258 cites W2410492149 @default.
- W2029863258 cites W334415753 @default.
- W2029863258 cites W55815732 @default.
- W2029863258 cites W76465934 @default.
- W2029863258 cites W80130412 @default.
- W2029863258 cites W1979238253 @default.
- W2029863258 doi "https://doi.org/10.1046/j.1365-2567.1997.00371.x" @default.
- W2029863258 hasPubMedCentralId "https://www.ncbi.nlm.nih.gov/pmc/articles/1364153" @default.
- W2029863258 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/9497489" @default.
- W2029863258 hasPublicationYear "1997" @default.
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