Age-related macular degeneration and the immune response: Implications for therapy

被引:105
作者
Nussenblatt, Robert B.
Ferris, Frederick, III
机构
[1] NEI, Lab Immunol, NIH, Bethesda, MD 20892 USA
[2] NEI, Div Epidemiol & Clin Res, NIH, Bethesda, MD 20892 USA
关键词
D O I
10.1016/j.ajo.2007.06.025
中图分类号
R77 [眼科学];
学科分类号
100212 ;
摘要
PURPOSE: To review the available information concerning the immune mediation of age-related macular degeneration (AMD) and to speculate on proposed mechanisms and immunotherapy. DESIGN: Interpretative essay. METHODS: Literature review and interpretation. RESULTS: An ever-growing body of evidence is gathering concerning the role of the immune system in AMD. Evidence to date suggests that the underlying mechanism leading to AMD is the decline of the ocular downregulatory immune environment. The subsequent activation of the immune system would lead to T-cell sensitization. When combined with local antiangiogenic therapy, several existing immunotherapies may be used to downregulate the immune response, potentially leading to a more efficient inhibition of choroidal neovascularization. CONCLUSIONS: The loss of the downregulatory immune environment is central to the development of AMD, permitting activation of the immune system. If so, immunotherapy could positively alter the course of the disease.
引用
收藏
页码:618 / 626
页数:9
相关论文
共 87 条
[21]   Macrophage depletion diminishes lesion size and severity in experimental choroidal Neovascularization [J].
Espinosa-Heidmann, DG ;
Suner, IJ ;
Hernandez, EP ;
Monroy, D ;
Csaky, KG ;
Cousins, SW .
INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE, 2003, 44 (08) :3586-3592
[22]   Oral tolerance [J].
Faria, AMC ;
Weiner, HL .
IMMUNOLOGICAL REVIEWS, 2005, 206 :232-259
[23]  
Ferris FL, 2005, ARCH OPHTHALMOL-CHIC, V123, P1570
[24]  
Friedman DS, 2004, ARCH OPHTHALMOL-CHIC, V122, P564
[25]   Age-related macular degeneration - emerging pathogenetic and therapeutic concepts [J].
Gehrs, Karen M. ;
Anderson, Don H. ;
Johnson, Lincoln V. ;
Hageman, Gregory S. .
ANNALS OF MEDICINE, 2006, 38 (07) :450-471
[26]   Variation in factor B (BF) and complement component 2 (C2) genes is associated with age-related macular degeneration [J].
Gold, B ;
Merriam, JE ;
Zernant, J ;
Hancox, LS ;
Taiber, AJ ;
Gehrs, K ;
Cramer, K ;
Neel, J ;
Bergeron, J ;
Barile, GR ;
Smith, RT ;
Dean, M ;
Allikmets, R .
NATURE GENETICS, 2006, 38 (04) :458-462
[27]   Monocyte and macrophage heterogeneity [J].
Gordon, S ;
Taylor, PR .
NATURE REVIEWS IMMUNOLOGY, 2005, 5 (12) :953-964
[28]   Macrophage heterogeneity and tissue lipids [J].
Gordon, Siamon .
JOURNAL OF CLINICAL INVESTIGATION, 2007, 117 (01) :89-93
[29]   No association between complement factor H gene polymorphism and exudative age-related macular degeneration in Japanese [J].
Gotoh, Norimoto ;
Yamada, Ryo ;
Hiratani, Hitomi ;
Renault, Victor ;
Kuroiwa, Sachiko ;
Monet, Marion ;
Toyoda, Sachiko ;
Chida, Shohei ;
Mandai, Michiko ;
Otani, Atsushi ;
Yoshimura, Nagahisa ;
Matsuda, Fumihiko .
HUMAN GENETICS, 2006, 120 (01) :139-143
[30]   Ethnic variation in AMD-associated complement factor H polymorphism p.Tyr402His [J].
Grassi, Michael A. ;
Fingert, John H. ;
Scheetz, Todd E. ;
Roos, Benjamin R. ;
Ritch, Robert ;
West, Sheila K. ;
Kawase, Kazuhide ;
Shire, Abdirashid M. ;
Mullins, Robert E. ;
Stone, Edwin M. .
HUMAN MUTATION, 2006, 27 (09) :921-925