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Peripheral tissue chemokines: homeostatic control of immune surveillance T cells.

McCully, Michelle L., Kouzeli, Ariadni, Moser, Bernhard·2018·Trends in Immunology
DOI 10.1016/j.it.2018.06.003
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Abstract

Cellular immunity is governed by a complex network of migratory cues that enable appropriate immune cell responses in a timely and spatially controlled fashion. This review focuses on the chemokines and their receptors regulating the steady-state localisation of immune cells within healthy peripheral tissues. Steady-state immune cell traffic is not well understood but is thought to involve constitutive (homeostatic) chemokines. The recent discovery of tissue-resident memory T cells (T RM cells) illustrates our need for understanding how chemokines control immune cell mobilisation and/or retention. These studies will be critical to unravel novel pathways for preserving tissue function (aging) and preventing tissue disease (vaccination).

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  • Immune regulators promote better surveillance and wound clearance in multiple tissues.

    “Immune regulators promote better surveillance and wound clearance in multiple tissues [75, 76].”

    From Rejuvenation of three germ layers tissues by exchanging old blood plasma with saline-albumin (2020) · cites this paper as [76]

    The Highlights (p. 27) say peripheral-tissue chemokines orchestrate local immune surveillance, and the Concluding Remarks (p. 13) describe their role in retaining surveillance cells in tissues such as skin and mucosal epithelia. Our copy does not say they promote wound clearance; its discussion of tissue recovery concerns the resolution of infection and inflammation, not wounds. (LLM, conf=0.85)

    Experimental — accuracy not yet measured

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Research works printed but not linked: 132

  1. Zlotnik, 2012, The chemokine superfamily revisited, Immunity, 36, 705, 10.1016/j.immuni.2012.05.008 · DOI
  2. Griffith, 2014, Chemokines and chemokine receptors: positioning cells for host defense and immunity, Annu. Rev. Immunol., 32, 659, 10.1146/annurev-immunol-032713-120145 · DOI
  3. Schulz, 2016, Chemokines and chemokine receptors in lymphoid tissue dynamics, Annu. Rev. Immunol., 34, 203, 10.1146/annurev-immunol-041015-055649 · DOI
  4. Amit, 2016, The role of the local environment and epigenetics in shaping macrophage identity and their effect on tissue homeostasis, Nat. Immunol., 17, 18, 10.1038/ni.3325 · DOI
  5. Mueller, 2013, Memory T cell subsets, migration patterns, and tissue residence, Annu. Rev. Immunol., 31, 137, 10.1146/annurev-immunol-032712-095954 · DOI
  6. Park, 2015, The emerging role of resident memory T cells in protective immunity and inflammatory disease, Nat. Med., 21, 688, 10.1038/nm.3883 · DOI
  7. Sallusto, 1999, Two subsets of memory T lymphocytes with distinct homing potentials and effector functions, Nature, 401, 708, 10.1038/44385 · DOI · Paper page
  8. Sallusto, 2000, Understanding dendritic cell and T-lymphocyte traffic through the analysis of chemokine receptor expression, Immunol. Rev., 177, 134, 10.1034/j.1600-065X.2000.17717.x · DOI
  9. Masopust, 2004, Activated primary and memory CD8 T cells migrate to nonlymphoid tissues regardless of site of activation or tissue of origin, J. Immunol., 172, 4875, 10.4049/jimmunol.172.8.4875 · DOI
  10. Yu, 2017, Epigenetic landscapes reveal transcription factors that regulate CD8(+) T cell differentiation, Nat. Immunol., 18, 573, 10.1038/ni.3706 · DOI
  11. Pace, 2018, The epigenetic control of stemness in CD8(+) T cell fate commitment, Science, 359, 177, 10.1126/science.aah6499 · DOI
  12. Moser, 2004, Chemokines: multiple levels of leukocyte migration control, Trends Immunol., 25, 75, 10.1016/j.it.2003.12.005 · DOI
  13. Ginhoux, 2016, New insights into the multidimensional concept of macrophage ontogeny, activation and function, Nat. Immunol., 17, 34, 10.1038/ni.3324 · DOI
  14. Okabe, 2016, Tissue biology perspective on macrophages, Nat. Immunol., 17, 9, 10.1038/ni.3320 · DOI
  15. McCully, 2011, The human cutaneous chemokine system, Front. Immunol., 2, 1, 10.3389/fimmu.2011.00033 · DOI
  16. Bachelerie, 2014, International Union of Basic and Clinical Pharmacology. [corrected]. LXXXIX. Update on the extended family of chemokine receptors and introducing a new nomenclature for atypical chemokine receptors, Pharmacol. Rev., 66, 1, 10.1124/pr.113.007724 · DOI
  17. Loetscher, 2000, Chemokines and their receptors in lymphocyte traffic and HIV infection, Adv. Immunol., 74, 127, 10.1016/S0065-2776(08)60910-4 · DOI
  18. Nagasawa, 2014, CXC chemokine ligand 12 (CXCL12) and its receptor CXCR4, J. Mol. Med., 92, 433, 10.1007/s00109-014-1123-8 · DOI
  19. Luo, 2016, Role of stromal-derived factor-1 in mesenchymal stem cell paracrine-mediated tissue repair, Curr. Stem Cell Res. Ther., 11, 585, 10.2174/1574888X11666160614102629 · DOI
  20. Graham, 2012, The biochemistry and biology of the atypical chemokine receptors, Immunol. Lett., 145, 30, 10.1016/j.imlet.2012.04.004 · DOI
  21. Mackay, 2017, Transcriptional regulation of tissue-resident lymphocytes, Trends Immunol., 38, 94, 10.1016/j.it.2016.11.004 · DOI
  22. Stelma, 2017, Human intrahepatic CD69+CD8+ T cells have a tissue resident memory T cell phenotype with reduced cytolytic capacity, Sci. Rep., 7, 6172, 10.1038/s41598-017-06352-3 · DOI
  23. Lunemann, 2017, Hobit expression by a subset of human liver-resident CD56(bright) Natural Killer cells, Sci. Rep., 7, 6676, 10.1038/s41598-017-06011-7 · DOI
  24. Zaid, 2017, Chemokine receptor-dependent control of skin tissue-resident memory T cell formation, J. Immunol., 199, 2451, 10.4049/jimmunol.1700571 · DOI
  25. Scholz, 2007, Constitutive expression and regulated release of the transmembrane chemokine CXCL16 in human and murine skin, J. Invest. Dermatol., 127, 1444, 10.1038/sj.jid.5700751 · DOI
  26. Gunther, 2012, CXCL16 and CXCR6 are upregulated in psoriasis and mediate cutaneous recruitment of human CD8+ T cells, J. Invest. Dermatol., 132, 626, 10.1038/jid.2011.371 · DOI
  27. Homey, 2000, Up-regulation of macrophage inflammatory protein-3 alpha/CCL20 and CC chemokine receptor 6 in psoriasis, J. Immunol., 164, 6621, 10.4049/jimmunol.164.12.6621 · DOI
  28. Kwon, 2002, Colonic epithelial cells are a major site of macrophage inflammatory protein 3alpha (MIP-3alpha) production in normal colon and inflammatory bowel disease, Gut, 51, 818, 10.1136/gut.51.6.818 · DOI
  29. Cai, 2011, Pivotal role of dermal IL-17-producing gammadelta T cells in skin inflammation, Immunity, 35, 596, 10.1016/j.immuni.2011.08.001 · DOI
  30. Hartwig, 2015, Dermal IL-17-producing gammadelta T cells establish long-lived memory in the skin, Eur. J. Immunol., 45, 3022, 10.1002/eji.201545883 · DOI
  31. Ramirez-Valle, 2015, Inflammation induces dermal Vgamma4+ gammadeltaT17 memory-like cells that travel to distant skin and accelerate secondary IL-17-driven responses, Proc. Natl. Acad. Sci. U. S. A., 112, 8046, 10.1073/pnas.1508990112 · DOI
  32. Zhang, 2016, Migratory and adhesive cues controlling innate-like lymphocyte surveillance of the pathogen-exposed surface of the lymph node, Elife, 5, 10.7554/eLife.18156 · DOI
  33. Mowat, 2014, Regional specialization within the intestinal immune system, Nat. Rev. Immunol., 14, 667, 10.1038/nri3738 · DOI
  34. Marsal, 2012, Targeting T-cell migration in inflammatory bowel disease, J. Intern. Med., 272, 411, 10.1111/j.1365-2796.2012.02588.x · DOI
  35. Homey, 2000, Cutting edge: the orphan chemokine receptor G protein-coupled receptor-2 (GPR-2, CCR10) binds the skin-associated chemokine CCL27 (CTACK/ALP/ILC), J. Immunol., 164, 3465, 10.4049/jimmunol.164.7.3465 · DOI
  36. Wang, 2000, Identification of a novel chemokine (CCL28), which binds CCR10 (GPR2), J. Biol. Chem., 275, 22313, 10.1074/jbc.M001461200 · DOI
  37. Ishikawa-Mochizuki, 1999, Molecular cloning of a novel CC chemokine, interleukin-11 receptor α-locus chemokine (ILC), which is located on chromosome 9p13 and a potential homologue of a CC chemokine encoded by molluscum contagiosum virus, FEBS Lett., 460, 544, 10.1016/S0014-5793(99)01406-4 · DOI
  38. Morales, 1999, CTACK, a skin-associated chemokine that preferentially attracts skin-homing memory T cells, Proc. Natl. Acad. Sci. U. S. A., 96, 14470, 10.1073/pnas.96.25.14470 · DOI
  39. Homey, 2002, CCL27-CCR10 interactions regulate T cell-mediated skin inflammation, Nat. Med., 8, 157, 10.1038/nm0202-157 · DOI
  40. Pan, 2000, A novel chemokine ligand for CCR10 and CCR3 expressed by epithelial cells in mucosal tissues, J. Immunol., 165, 2943, 10.4049/jimmunol.165.6.2943 · DOI
  41. Hernandez-Ruiz, 2017, Mucosal chemokines, J. Interferon Cytokine Res., 37, 62, 10.1089/jir.2016.0076 · DOI
  42. Matsuo, 2018, CCL28-deficient mice have reduced IgA antibody-secreting cells and an altered microbiota in the colon, J. Immunol., 200, 800, 10.4049/jimmunol.1700037 · DOI
  43. Morteau, 2008, An indispensable role for the chemokine receptor CCR10 in IgA antibody-secreting cell accumulation, J. Immunol., 181, 6309, 10.4049/jimmunol.181.9.6309 · DOI
  44. Danilova, 2015, A role for CCL28-CCR3 in T-cell homing to the human upper airway mucosa, Mucosal Immunol., 8, 107, 10.1038/mi.2014.46 · DOI
  45. Reiss, 2001, CC chemokine receptor (CCR)4 and the CCR10 ligand cutaneous T cell-attracting chemokine (CTACK) in lymphocyte trafficking to inflamed skin, J. Exp. Med., 194, 1541, 10.1084/jem.194.10.1541 · DOI
  46. Xia, 2014, CCR10 regulates balanced maintenance and function of resident regulatory and effector T cells to promote immune homeostasis in the skin, J. Allergy Clin. Immunol., 134, 10.1016/j.jaci.2014.03.010 · DOI · Paper page
  47. Yang, 2016, Selective programming of CCR10(+) innate lymphoid cells in skin-draining lymph nodes for cutaneous homeostatic regulation, Nat. Immunol., 17, 48, 10.1038/ni.3312 · DOI · Paper page
  48. Regoli, 2017, The multifaceted personality of intestinal CX3CR1(+) macrophages, Trends Immunol., 38, 879, 10.1016/j.it.2017.07.009 · DOI
  49. Gerlach, 2016, The chemokine receptor CX3CR1 defines three antigen-experienced CD8 T cell subsets with distinct roles in immune surveillance and homeostasis, Immunity, 45, 1270, 10.1016/j.immuni.2016.10.018 · DOI · Paper page
  50. Bottcher, 2015, Functional classification of memory CD8(+) T cells by CX3CR1 expression, Nat. Commun., 6, 8306, 10.1038/ncomms9306 · DOI
  51. Konkel, 2017, Transforming growth factor-beta signaling in regulatory T cells controls T helper-17 cells and tissue-specific immune responses, Immunity, 46, 660, 10.1016/j.immuni.2017.03.015 · DOI
  52. Lahl, 2014, Orphan chemoattractant receptor GPR15 mediates dendritic epidermal T-cell recruitment to the skin, Eur. J. Immunol., 44, 2577, 10.1002/eji.201444628 · DOI
  53. Nguyen, 2015, Role and species-specific expression of colon T cell homing receptor GPR15 in colitis, Nat. Immunol., 16, 207, 10.1038/ni.3079 · DOI
  54. Kim, 2013, GPR15-mediated homing controls immune homeostasis in the large intestine mucosa, Science, 340, 1456, 10.1126/science.1237013 · DOI
  55. Pan, 2017, The fifth epidermal growth factor like region of thrombomodulin alleviates LPS-induced sepsis through interacting with GPR15, Thromb. Haemost., 117, 570, 10.1160/TH16-10-0762 · DOI
  56. Suply, 2017, A natural ligand for the orphan receptor GPR15 modulates lymphocyte recruitment to epithelia, Sci. Signal., 10, 10.1126/scisignal.aal0180 · DOI
  57. Lu, 2016, CXCL14 as an emerging immune and inflammatory modulator, J. Inflamm. (Lond), 13, 1, 10.1186/s12950-015-0109-9 · DOI
  58. Meuter, 2007, Murine CXCL14 is dispensable for dendritic cell function and localization within peripheral tissues, Mol. Cell Biol., 27, 983, 10.1128/MCB.01648-06 · DOI
  59. Nara, 2007, Disruption of CXC motif chemokine ligand-14 in mice ameliorates obesity-induced insulin resistance, J. Biol. Chem., 282, 30794, 10.1074/jbc.M700412200 · DOI · Paper page
  60. Tanegashima, 2010, CXCL14 deficiency in mice attenuates obesity and inhibits feeding behavior in a novel environment, PLoS One, 5, 10.1371/journal.pone.0010321 · DOI
  61. Collins, 2017, Epithelial chemokine CXCL14 synergizes with CXCL12 via allosteric modulation of CXCR4, FASEB J., 31, 3084, 10.1096/fj.201700013R · DOI
  62. Burkhardt, 2014, CXCL17 is a major chemotactic factor for lung macrophages, J. Immunol., 193, 1468, 10.4049/jimmunol.1400551 · DOI
  63. Oka, 2017, CXCL17 Attenuates imiquimod-induced psoriasis-like skin inflammation by recruiting myeloid-derived suppressor cells and regulatory T cells, J. Immunol., 198, 3897, 10.4049/jimmunol.1601607 · DOI
  64. Maravillas-Montero, 2015, Cutting edge: GPR35/CXCR8 is the receptor of the mucosal chemokine CXCL17, J. Immunol., 194, 29, 10.4049/jimmunol.1401704 · DOI
  65. Park, 2018, GPR35 mediates lodoxamide-induced migration inhibitory response but not CXCL17-induced migration stimulatory response in THP-1 cells; is GPR35 a receptor for CXCL17?, Br. J. Pharmacol., 175, 154, 10.1111/bph.14082 · DOI
  66. Tan, 2017, Metabolite-sensing G protein-coupled receptors-facilitators of diet-related immune regulation, Annu. Rev. Immunol., 35, 371, 10.1146/annurev-immunol-051116-052235 · DOI
  67. McCully, 2018, CCR8 expression defines tissue-resident memory T cells in human skin, J. Immunol., 200, 1639, 10.4049/jimmunol.1701377 · DOI
  68. Clark, 2006, The vast majority of CLA+ T cells are resident in normal skin, J. Immunol., 176, 4431, 10.4049/jimmunol.176.7.4431 · DOI · Paper page
  69. Bromley, 2013, Recirculating memory T cells are a unique subset of CD4+ T cells with a distinct phenotype and migratory pattern, J. Immunol., 190, 970, 10.4049/jimmunol.1202805 · DOI
  70. Scharschmidt, 2015, A wave of regulatory T cells into neonatal skin mediates tolerance to commensal microbes, Immunity, 43, 1011, 10.1016/j.immuni.2015.10.016 · DOI · Paper page
  71. Sanchez Rodriguez, 2014, Memory regulatory T cells reside in human skin, J. Clin. Invest., 124, 1027, 10.1172/JCI72932 · DOI
  72. Tomura, 2010, Activated regulatory T cells are the major T cell type emigrating from the skin during a cutaneous immune response in mice, J. Clin. Invest., 120, 883, 10.1172/JCI40926 · DOI
  73. Colantonio, 2002, Skin-homing CLA+ T cells and regulatory CD25+ T cells represent major subsets of human peripheral blood memory T cells migrating in response to CCL1/I-309, Eur. J. Immunol., 32, 3506, 10.1002/1521-4141(200212)32:12<3506::AID-IMMU3506>3.0.CO;2-# · DOI
  74. Plitas, 2016, Regulatory T cells exhibit distinct features in human breast cancer, Immunity, 45, 1122, 10.1016/j.immuni.2016.10.032 · DOI · Paper page
  75. De Simone, 2016, Transcriptional landscape of human tissue lymphocytes unveils uniqueness of tumor-infiltrating T regulatory cells, Immunity, 45, 1135, 10.1016/j.immuni.2016.10.021 · DOI · Paper page
  76. Barsheshet, 2017, CCR8+FOXp3+ Treg cells as master drivers of immune regulation, Proc. Natl. Acad. Sci. U. S. A., 114, 6086, 10.1073/pnas.1621280114 · DOI
  77. Hoelzinger, 2010, Blockade of CCL1 inhibits T regulatory cell suppressive function enhancing tumor immunity without affecting T effector responses, J. Immunol., 184, 6833, 10.4049/jimmunol.0904084 · DOI
  78. Asai, 2012, CCL1 released from M2b macrophages is essentially required for the maintenance of their properties, J. Leukoc. Biol., 92, 859, 10.1189/jlb.0212107 · DOI · Paper page
  79. Islam, 2011, Mouse CCL8, a CCR8 agonist, promotes atopic dermatitis by recruiting IL-5+ T(H)2 cells, Nat. Immunol., 12, 167, 10.1038/ni.1984 · DOI
  80. Mora, 2006, T-cell homing specificity and plasticity: new concepts and future challenges, Trends Immunol., 27, 235, 10.1016/j.it.2006.03.007 · DOI
  81. Sigmundsdottir, 2008, Environmental cues, dendritic cells and the programming of tissue-selective lymphocyte trafficking, Nat. Immunol., 9, 981, 10.1038/ni.f.208 · DOI
  82. McCully, 2012, Epidermis instructs skin homing receptor expression in human T cells, Blood, 120, 4591, 10.1182/blood-2012-05-433037 · DOI
  83. McCully, 2015, Skin metabolites define a new paradigm in the localization of skin tropic memory T cells, J. Immunol., 195, 96, 10.4049/jimmunol.1402961 · DOI
  84. Sigmundsdottir, 2007, DCs metabolize sunlight-induced vitamin D3 to ‘program’ T cell attraction to the epidermal chemokine CCL27, Nat. Immunol., 8, 285, 10.1038/ni1433 · DOI
  85. Agace, 2012, How vitamin A metabolizing dendritic cells are generated in the gut mucosa, Trends Immunol., 33, 42, 10.1016/j.it.2011.10.001 · DOI
  86. Iwata, 2004, Retinoic acid imprints gut-homing specificity on T cells, Immunity, 21, 527, 10.1016/j.immuni.2004.08.011 · DOI · Paper page
  87. Mora, 2006, Generation of gut-homing IgA-secreting B cells by intestinal dendritic cells, Science, 314, 1157, 10.1126/science.1132742 · DOI
  88. Kim, 2015, Retinoic acid differentially regulates the migration of innate lymphoid cell subsets to the gut, Immunity, 43, 107, 10.1016/j.immuni.2015.06.009 · DOI
  89. Rosas, 2014, The transcription factor Gata6 links tissue macrophage phenotype and proliferative renewal, Science, 344, 645, 10.1126/science.1251414 · DOI
  90. Okabe, 2014, Tissue-specific signals control reversible program of localization and functional polarization of macrophages, Cell, 157, 832, 10.1016/j.cell.2014.04.016 · DOI · Paper page
  91. Urry, 2012, The role of 1alpha,25-dihydroxyvitamin D3 and cytokines in the promotion of distinct Foxp3+ and IL-10+ CD4+ T cells, Eur. J. Immunol., 42, 2697, 10.1002/eji.201242370 · DOI
  92. Bakdash, 2015, Retinoic acid primes human dendritic cells to induce gut-homing, IL-10-producing regulatory T cells, Mucosal Immunol., 8, 265, 10.1038/mi.2014.64 · DOI
  93. van der Aar, 2011, Vitamin D3 targets epidermal and dermal dendritic cells for induction of distinct regulatory T cells, J. Allergy Clin. Immunol., 127, 10.1016/j.jaci.2011.01.068 · DOI
  94. Pan, 2017, Survival of tissue-resident memory T cells requires exogenous lipid uptake and metabolism, Nature, 543, 252, 10.1038/nature21379 · DOI
  95. Casey, 2012, Antigen-independent differentiation and maintenance of effector-like resident memory T cells in tissues, J. Immunol., 188, 4866, 10.4049/jimmunol.1200402 · DOI
  96. Mackay, 2015, T-box transcription factors combine with the cytokines TGF-beta and IL-15 to control tissue-resident memory T cell fate, Immunity, 43, 1101, 10.1016/j.immuni.2015.11.008 · DOI
  97. Iijima, 2014, T cell memory. A local macrophage chemokine network sustains protective tissue-resident memory CD4 T cells, Science, 346, 93, 10.1126/science.1257530 · DOI · Paper page
  98. Ariotti, 2012, Tissue-resident memory CD8+ T cells continuously patrol skin epithelia to quickly recognize local antigen, Proc. Natl. Acad. Sci. U. S. A., 109, 19739, 10.1073/pnas.1208927109 · DOI
  99. Beura, 2018, Intravital mucosal imaging of CD8(+) resident memory T cells shows tissue-autonomous recall responses that amplify secondary memory, Nat. Immunol., 19, 173, 10.1038/s41590-017-0029-3 · DOI
  100. Miller, 1989, A novel polypeptide secreted by activated human T lymphocytes, J. Immunol., 143, 2907, 10.4049/jimmunol.143.9.2907 · DOI
  101. Burd, 1987, Cloning and characterization of a novel T cell activation gene, J. Immunol., 139, 3126, 10.4049/jimmunol.139.9.3126 · DOI
  102. Miller, 1992, The human cytokine I-309 is a monocyte chemoattractant, Proc. Natl. Acad. Sci. U. S. A., 89, 2950, 10.1073/pnas.89.7.2950 · DOI
  103. Tiffany, 1997, Identification of CCR8: A human monocyte and thymus receptor for the CC chemokine I-309, J. Exp. Med., 186, 165, 10.1084/jem.186.1.165 · DOI
  104. Roos, 1997, Identification of CCR8, the receptor for the human CC chemokine I-309, J. Biol. Chem., 272, 17251, 10.1074/jbc.272.28.17251 · DOI
  105. Goya, 1998, Identification of CCR8 as the specific receptor for the human β-chemokine I-309: Cloning and molecular characterization of murine CCR8 as the receptor for TCA-3, J. Immunol., 160, 1975, 10.4049/jimmunol.160.4.1975 · DOI
  106. Islam, 2013, Identification of human CCR8 as a CCL18 receptor, J. Exp. Med., 210, 1889, 10.1084/jem.20130240 · DOI
  107. Goya, 2003, Absence of CCR8 does not impair the response to ovalbumin-induced allergic airway disease, J. Immunol., 170, 2138, 10.4049/jimmunol.170.4.2138 · DOI
  108. Chung, 2003, CCR8 is not essential for the development of inflammation in a mouse model of allergic airway disease, J. Immunol., 170, 581, 10.4049/jimmunol.170.1.581 · DOI
  109. Chensue, 2001, Aberrant in vivo T helper type 2 cell response and impaired eosinophil recruitment in CC chemokine receptor 8 knockout mice, J. Exp. Med., 193, 573, 10.1084/jem.193.5.573 · DOI
  110. Buckland, 2007, Remission of chronic fungal asthma in the absence of CCR8, J. Allergy Clin. Immunol., 119, 997, 10.1016/j.jaci.2006.12.660 · DOI
  111. Qu, 2004, Role of CCR8 and other chemokine pathways in the migration of monocyte-derived dendritic cells to lymph nodes, J. Exp. Med., 200, 1231, 10.1084/jem.20032152 · DOI
  112. Yabe, 2015, CCR8 regulates contact hypersensitivity by restricting cutaneous dendritic cell migration to the draining lymph nodes, Int. Immunol., 27, 169, 10.1093/intimm/dxu098 · DOI
  113. Nagao, 2012, Stress-induced production of chemokines by hair follicles regulates the trafficking of dendritic cells in skin, Nat. Immunol., 13, 744, 10.1038/ni.2353 · DOI
  114. Annunziato, 1998, Molecules associated with human Th1 or Th2 cells, Eur. Cytokine Netw., 9, 12
  115. D’Ambrosio, 1998, Selective up-regulation of chemokine receptors CCR4 and CCR8 upon activation of polarized human type 2 Th cells, J. Immunol., 161, 5111, 10.4049/jimmunol.161.10.5111 · DOI
  116. Zingoni, 1998, The chemokine receptor CCR8 is preferentially expressed in Th2 but not Th1 cells, J. Immunol., 161, 547, 10.4049/jimmunol.161.2.547 · DOI · Paper page
  117. Panina-Bordignon, 2001, The C-C chemokine receptors CCR4 and CCR8 identify airway T cells of allergen-challenged atopic asthmatics, J. Clin. Invest., 107, 1357, 10.1172/JCI12655 · DOI
  118. Sebastiani, 2001, Chemokine receptor expression and function in CD4+ T lymphocytes with regulatory activity, J. Immunol., 166, 996, 10.4049/jimmunol.166.2.996 · DOI
  119. Gombert, 2005, CCL1-CCR8 interactions: an axis mediating the recruitment of T cells and Langerhans-type dendritic cells to sites of atopic skin inflammation, J. Immunol., 174, 5082, 10.4049/jimmunol.174.8.5082 · DOI
  120. Gonzalo, 2007, Coordinated involvement of mast cells and T cells in allergic mucosal inflammation: critical role of the CC chemokine ligand 1:CCR8 axis, J. Immunol., 179, 1740, 10.4049/jimmunol.179.3.1740 · DOI
  121. Soler, 2006, CCR8 expression identifies CD4 memory T cells enriched for FOXP3+ regulatory and Th2 effector lymphocytes, J. Immunol., 177, 6940, 10.4049/jimmunol.177.10.6940 · DOI
  122. Coghill, 2013, CC chemokine receptor 8 potentiates donor Treg survival and is critical for the prevention of murine graft-versus-host disease, Blood, 122, 825, 10.1182/blood-2012-06-435735 · DOI
  123. Ebert, 2006, Homing and function of human skin gammadelta T cells and NK cells: relevance for tumor surveillance, J. Immunol., 176, 4331, 10.4049/jimmunol.176.7.4331 · DOI
  124. Schaerli, 2004, A skin-selective homing mechanism for human immune surveillance T cells, J. Exp. Med., 199, 1265, 10.1084/jem.20032177 · DOI
  125. Mutalithas, 2010, Expression of CCR8 is increased in asthma, Clin. Exp. Allergy, 40, 1175, 10.1111/j.1365-2222.2010.03504.x · DOI
  126. Nakajima, 2002, Marked increase in CC chemokine gene expression in both human and mouse mast cell transcriptomes following Fcepsilon receptor I cross-linking: an interspecies comparison, Blood, 100, 3861, 10.1182/blood-2002-02-0602 · DOI
  127. Gilchrest, 2003, Human cord blood-derived mast cells synthesize and release I-309 in response to IgE, Life Sci., 73, 2571, 10.1016/S0024-3205(03)00607-6 · DOI
  128. N’Diaye, 2006, Aryl hydrocarbon receptor- and calcium-dependent induction of the chemokine CCL1 by the environmental contaminant benzo[a]pyrene, J. Biol. Chem., 281, 19906, 10.1074/jbc.M601192200 · DOI
  129. Hoshino, 2007, Inhibition of CCL1-CCR8 interaction prevents aggregation of macrophages and development of peritoneal adhesions, J. Immunol., 178, 5296, 10.4049/jimmunol.178.8.5296 · DOI
  130. Das, 2013, Tumor cell entry into the lymph node is controlled by CCL1 chemokine expressed by lymph node lymphatic sinuses, J. Exp. Med., 210, 1509, 10.1084/jem.20111627 · DOI
  131. Lüttichau, 2000, A highly selective CC chemokine receptor (CCR)8 antagonist encoded by the poxvirus molluscum contagiosum, J. Exp. Med., 191, 171, 10.1084/jem.191.1.171 · DOI
  132. Kledal, 1997, A broad-spectrum chemokine antagonist encoded by Kaposi’s sarcoma-associated herpesvirus, Science, 277, 1656, 10.1126/science.277.5332.1656 · DOI

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Metadata

Authors
McCully, M. L., Kouzeli, A., & Moser, B.
Venue
Trends in Immunology
Publisher
Elsevier BV
Published
2018-09
Volume
39
Issue
9
Pages
734-747
ISSN
1471-4906
DOI
10.1016/j.it.2018.06.003
Cited by
37
References
15
Language
en
Licence
www.elsevier.com/tdm/userlicense/1.0/ (tdm)

About these checks

Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.

Statistics and arithmetic are recomputed, not judged.

Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.

What counts as a claim ›How we measure confidence ›How we check this ›

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