2002
DOI: 10.1016/s0531-5565(01)00205-4
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Immunosenescence of macrophages: reduced MHC class II gene expression

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Cited by 103 publications
(55 citation statements)
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“…These data indicate that proinflammatory cytokine responses decline with aging when TLR2, 3, 4, 5, and 9 on splenic or thioglycollate-elicited macrophages are stimulated with their ligands. TNF-␣ enhances class I and class II MHC expression and decreased levels in aging could affect Ag processing and presentation, thus affecting T cell responses (22). Reduced TNF-␣ levels in aging may also contribute to reduced phagocytic activity, reduced NO, reduced tumor cell killing, and delayed tissue repair process.…”
Section: Resultsmentioning
confidence: 99%
“…These data indicate that proinflammatory cytokine responses decline with aging when TLR2, 3, 4, 5, and 9 on splenic or thioglycollate-elicited macrophages are stimulated with their ligands. TNF-␣ enhances class I and class II MHC expression and decreased levels in aging could affect Ag processing and presentation, thus affecting T cell responses (22). Reduced TNF-␣ levels in aging may also contribute to reduced phagocytic activity, reduced NO, reduced tumor cell killing, and delayed tissue repair process.…”
Section: Resultsmentioning
confidence: 99%
“…Macrophages/monocytes. Even though the number and phagocytic activity of macrophages is unchanged with age, impaired antigen presentation and reduced MHC II molecule expression have been demonstrated in macrophages from aged mice (47). However, after activation by mitogen, peripheral blood mononuclear cells from older persons produce more proinflammatory cytokines such as IL-1, IL-6, and TNF-a in vitro than those from younger ones (48,49).…”
Section: Aging-related Changes To the Innate Immune System-associatedmentioning
confidence: 99%
“…The impact of aging on the expression and function of many of these cell surface proteins is unclear. Aging human and rodent macrophage populations appear to have reduced levels of class II MHC, and it has been suggested that this may contribute to poor T-cell responses (Zissel et al ., 1999;Herrero et al ., 2002). The number of blood monocytes in the elderly and young subjects appears to be very similar; however, there is a significant decrease in the macrophage precursors as well as macrophages in the bone marrow of the elderly ( Takahashi et al ., 1985;Ogawa et al ., 2000).…”
Section: Ontogeny and Distribution Of Macrophagesmentioning
confidence: 99%