Resumen
Las células linfoides innatas (ILC) son linfocitos que carecen de receptores de reconocimiento de antígenos y se activan en respuesta a citocinas y a través de receptores de patrones moleculares asociados a microorganismos (MAMP). Las ILC se localizan preferentemente en las mucosas, y participan en la respuesta inmune contra infecciones y en enfermedades inflamatorias crónicas. Las ILC se dividen en ILC-1, ILC-2 e ILC-3, y estas células tienen funciones análogas a las de los linfocitos Th1, Th2 y Th17 de la respuesta inmune adaptativa. Las ILC-1 expresan T-bet, producen IFNγ, protegen contra infecciones con microorganismos intracelulares y están relacionados con la inmunopatología de la enfermedad inflamatoria intestinal. Las ILC-2 expresan GATA3, producen IL-4, IL-5, IL-13 y anfirregulina, protegen contra infecciones parasitarias y se relacionan con la inmunopatología de la alergia y la obesidad. Las ILC-3 expresan RORγt, producen IL-17 e IL-22, protegen contra infecciones con hongos y participan en la tolerancia a la microbiota intestinal y en la reparación intestinal. Se relacionan con la inmunopatología de la enfermedad inflamatoria intestinal y la psoriasis. En términos generales, las ILC mantienen la homeostasis y coadyuvan en la protección contra las infecciones.
Referencias
Rajamuthiah R, Mylonakis E. Effector triggered immunity. Virulence. 2014;5(7):697-702. DOI: http://dx.doi.org/10.4161/viru.29091
Netea MG, Latz E, Mills KH, O’Neill LA. Innate immune memory: a paradigm shift in understanding host defense. Nat Immunol. 2015;16(7):675-679. DOI: http://dx.doi.org/10.1038/ni.3178
Sonnenberg GF, Fouser LA, Artis D. Border patrol: Regulation of immunity, inflammation and tissue homeostasis at barrier surfaces by IL-22. Nat Immunol. 2011;12(5):383-390. DOI: http://dx.doi.org/10.1038/ni.2025
Inaba K, Steinman RM. Protein-specific helper T-lymphocyte formation initiated by dendritic cells. Science. 1985;229(4712):475-479. DOI: http://dx.doi.org/10.1126/science.3160115
Dumonde DC, Wolstencroft RA, Panayi GS, Matthew M, Morley J, Howson WT. “Lymphokines”: Non-antibody mediators of cellular immunity generated by lymphocyte activation. Nature. 1969;224(5214):38-42. DOI: http://dx.doi.org/10.1038/224038a0
Rosenau W, Moon HD. Lysis of homologous cells by sensitized lymphocytes in tissue culture. J Natl Cancer Inst. 1961;27(2):471-483. http://dx.doi.org/10.1093/jnci/27.2.471
Nossal GJV, Lederberg J. Antibody production by single cells. Nature. 1958;181(4620):1419-1420. DOI: http://dx.doi.org/10.1038/1811419a0
Jerne NK, Nordin AA. Plaque formation in Agar by single antibody-producing cells. Science. 1963;140(3565):405. DOI: http://dx.doi.org/10.1126/science.140.3565.405
Parkin J, Cohen B. An overview of the immune system. Lancet. 2001;357(9270):1777-1789. DOI: http://dx.doi.org/10.1016/S0140-6736(00)04904-7
Spits H, Artis D, Colonna M, Diefenbach A, Di Santo JP, Eberl G, et al. Innate lymphoid cells-a proposal for uniform nomenclature. Nat Rev Immunol. 2013;13(2):145-149. DOI: http://dx.doi.org/10.1038/nri3365
Spits H, Di-Santo JP. The expanding family of innate lymphoid cells: Regulators and effectors of immunity and tissue remodeling. Nat Immunol. 2011;12(1):21-27. DOI: http://dx.doi.org/10.1038/ni.1962
Eberl G. Development and evolution of RORgammat+ cells in a microbe’s world. Immunol Rev. 2012;245(1):177-188. DOI: http://dx.doi.org/10.1111/j.1600-065X.2011.01071.x
McKenzie ANJ, Spits H, Eberl G. Innate lymphoid cells in inflammation and immunity. Immunity. 2014;41(3):366-374. DOI: http://dx.doi.org/10.1016/j.immuni.2014.09.006
Kiessling R, Klein E, Wigzell H. “Natural” killer cells in the mouse. I. Cytotoxic cells with specificity for mouse Moloney leukemia cells. Specificity and distribution according to genotype. Eur J Immunol. 1975;5(2):112-117. DOI: http://dx.doi.org/10.1002/eji.1830050208
Kiessling R, Petranyi G, Kärre K, Jondal M, Tracey D, Wigzell H. Killer cells: A functional comparison between natural, immune T-cell and antibody-dependent in vitro systems. J Exp Med. 1976;143(4):772-780. DOI: http://dx.doi.org/10.1084/jem.143.4.772
Finke D. Fate and function of lymphoid tissue inducer cells. Curr Opin Immunol. 2005;17(2):144-150. DOI: http://dx.doi.org/10.1016/j.coi.2005.01.006
Kelly KA, Scollay R. Seeding of neonatal lymph nodes by T cells and identification of a novel population of CD3-CD4+ cells. Eur J Immunol. 1992;22(2):329-334. DOI: http://dx.doi.org/10.1002/eji.1830220207
Eberl G, Marmon S, Sunshine MJ, et al. An essential function for the nuclear receptor RORgamma(t) in the generation of fetal lymphoid tissue inducer cells. Nat Immunol. 2004;5(1):64-73. DOI: http://dx.doi.org/10.1038/ni1022
Satoh-Takayama N, Vosshenrich CA, Lesjean-Pottier S, Sawa S, Lochner M, Rattis F, et al. Microbial flora drives interleukin 22 production in intestinal NKp46+ cells that provide innate mucosal immune defense. Immunity. 2008;29(6):958-970. DOI: http://dx.doi.org/10.1016/j.immuni.2008.11.001
Cella M, Fuchs A, Vermi W, Facchetti F, Otero K, Lennerz JK, et al. A human natural killer cell subset provides an innate source of IL-22 for mucosal immunity. Nature. 2009;457(7230):722-725. DOI: http://dx.doi.org/10.1038/nature07537
Moro K, Yamada T, Tanabe M, Takeuchi T, Ikawa T, Kawamoto H, et al. Innate production of T(H)2 cytokines by adipose tissue-associated c-Kit(+)Sca-1(+) lymphoid cells. Nature. 2010;463(7280):540-544. DOI: http://dx.doi.org/10.1038/nature08636
Neill DR, Wong SH, Bellosi A, Flynn RJ, Daly Maria, Langford TKA, et al. Nuocytes represent a new innate effector leukocyte that mediates type-2 immunity. Nature. 2010;464(7293):1367-1370. DOI: http://dx.doi.org/10.1038/nature08900
Price AE, Liang HE, Sullivan BM, Reinhardt RL, Eisley CJ, Erle DJ, et al. Systemically dispersed innate IL-13-expressing cells in type 2 immunity. Proc Natl Acad Sci U S A. 2010;107(25):11489-11494. DOI: http://dx.doi.org/10.1073/pnas.1003988107
Klose CS, Flach M, Mohle L, Rogell L, Hoyler T, Ebert K, et al. Differentiation of type 1 ILCs from a common progenitor to all helper-like innate lymphoid cell lineages. Cell. 2014;157(2):340-356. DOI: http://dx.doi.org/10.1016/j.cell.2014.03.030
Serafini N, Vosshenrich CA, Di Santo JP. Transcriptional regulation of innate lymphoid cell fate. Nat Rev Immunol. 2015;15(7):415-428. DOI: http://dx.doi.org/10.1038/nri3855
Sonnenberg GF. Regulation of intestinal health and disease by innate lymphoid cells. Int Immunol. 2014;26(9):501-507. DOI: http://dx.doi.org/10.1093/intimm/dxu052
Krueger PD, Narayanan S, Surette FA, Brown MG, Sung SJ, Hahn YS. Murine liver-resident group 1 innate lymphoid cells regulate optimal priming of anti-viral CD8+ T cells. J Leukoc Biol. 2017;101(1):329-338. DOI: http://dx.doi.org/10.1189/jlb.3A0516-225R
Cortez VS, Robinette ML, Colonna M. Innate lymphoid cells: New insights into function and development. Curr Opin Immunol. 2015;32:71-77. DOI: http://dx.doi.org/10.1016/j.coi.2015.01.004
Monticelli LA, Sonnenberg GF, Abt MC, Alenghat T, Ziegler CG, Doering TA, et al. Innate lymphoid cells promote lung-tissue homeostasis after infection with influenza virus. Nat Immunol. 2011;12(11):1045-1054. DOI: http://dx.doi.org/10.1031/ni.2131
Carrega P, Loiacono F, Di Carlo E, Scaramuccia A, Mora M, Conte R, et al. NCR(+)ILC-3 concentrate in human lung cancer and associate with intratumoral lymphoid structures. Nat Commun. 2015;6:8280. DOI: http://dx.doi.org/10.1038/ncomms9280
Xu H, Wang X, Lackner AA, Veazey RS. Type 3 innate lymphoid cell depletion is mediated by TLRs in lymphoid tissues of simian immunodeficiency virus-infected macaques. FASEB J. 2015;29(12):5072-5080. DOI: http://dx.doi.org/10.1096/fj.15-276477
Spencer SP, Wilhelm C, Yang Q, Hall JA, Bouladoux N, Boyd A, et al. Adaptation of innate lymphoid cells to a micronutrient deficiency promotes type 2 barrier immunity. Science. 2014;343(6169):432-437. DOI: http://dx.doi.org/10.1126/science.1247606
Withers DR. Innate lymphoid cell regulation of adaptive immunity. Immunology. 2016;149(2):123-130. DOI: http://dx.doi.org/10.1111/imm.12639
Vély F, Barlogis V, Vallentin B, Neven B, Piperoglou C, Ebbo M, et al. Evidence of innate lymphoid cell redundancy in humans. Nat Immunol. 2016;17(11):1291-1299. DOI: http://dx.doi.org/10.1038/ni.3553
Diefenbach A. Innate lymphoid cells in the defense against infections. Eur J Microbiol Immunol (Bp). 2013;3(3):143-151. DOI: http://dx.doi.org/10.1556/EuJMI.3.2013.3.1
Eberl G, Colonna M, Di Santo JP, McKenzie AN. Innate lymphoid cells. Innate lymphoid cells: A new paradigm in immunology. Science. 2015;348(6237):aaa6566. DOI: http://dx.doi.org/10.1126/science.aaa6566
Erick TK, Brossay L. Phenotype and functions of conventional and non-conventional NK cells. Curr Opin Immunol. 2016;38:67-74. DOI: http://dx.doi.org/10.1016/j.coi.2015.11.007
Montel AH, Bochan MR, Hobbs JA, Lynch DH, Brahmi Z. Fas involvement in cytotoxicity mediated by human NK cells. Cell Immunol. 1995;166(2):236-246. DOI: http://dx.doi.org/10.1006/cimm.1995.9974
Poli A, Michel T, Théresine M, Andrès E, Hentges F, Zimmer J. CD56bright natural killer (NK) cells: An important NK cell subset. Immunology. 2009;126(4):458-465. DOI: http://dx.doi.org/10.1111/j.1365-2567.2008.03027.x
Spits H, Bernink JH, Lanier L. NK cells and type 1 innate lymphoid cells: Partners in host defense. Nat Immunol. 2016;17(7):758-764. DOI: http://dx.doi.org/10.1038/ni.3482
Hoyler T, Klose CS, Souabni A, Turqueti-Neves A, Pfeifer D, Rawlins EL, et al. The transcription factor GATA-3 controls cell fate and maintenance of type 2 innate lymphoid cells. Immunity. 2012;37(4):634-648. DOI: http://dx.doi.org/10.1016/j.immuni.2012.06.020
Kita H. ILC2s and fungal allergy. Allergol Int. 2015;64(3):219-226. DOI: http://dx.doi.org/10.1016/j.alit.2015.04.004
Juelke K, Romagnani C. Differentiation of human innate lymphoid cells (ILCs). Curr Opin Immunol. 2016;38:75-85. DOI: http://dx.doi.org/10.1016/j.coi.2015.11.005
Doherty TA, Khorram N, Lund S, Mehta AK, Croft M, Broide DH. Lung type 2 innate lymphoid cells express cysteinyl leukotriene receptor 1, which regulates TH2 cytokine production. J Allergy Clin Immunol. 2013;132(1):205-213. DOI: http://dx.doi.org/10.1016/j.jaci.2013.03.048
Barnig C, Cernadas M, Dutile S, Liu X, Perrella MA, Kazani S, et al. Lipoxin A4 regulates natural killer cell and type 2 innate lymphoid cell activation in asthma. Sci Transl Med. 2013;5(174):174ra126. DOI: http://dx.doi.org/10.1126/scitranslmed.3004812
Mjösberg J, Bernink J, Golebski K, Karrich JJ, Peters CP, Blom B, et al. The transcription factor GATA3 is essential for the function of human type 2 innate lymphoid cells. Immunity. 2012;37(4):649-659. DOI: http://dx.doi.org/10.1016/j.immuni.2012.08.015
Klein-Wolterink RG, Serafini N, Van-Nimwegen M, Vosshenrich CA, De-Bruijn MJ, Fonseca Pereira D, et al. Essential, dose-dependent role for the transcription factor Gata3 in the development of IL-5+ and IL-13+ type 2 innate lymphoid cells. Proc Natl Acad Sci U S A. 2013;110(25):10240-10245. DOI: http://dx.doi.org/10.1073/pnas.1217158110
Furusawa J, Moro K, Motomura Y, Okamoto K, Zhu J, Takayanagi H, et al. Critical role of p38 and GATA3 in natural helper cell function. J Immunol. 2013;191(4):1818-1826. DOI: http://dx.doi.org/10.4049/jimmunol.1300379
Takatori H, Kanno Y, Watford WT, Tato CM, Weiss G, Ivanov II, et al. Lymphoid tissue inducer-like cells are an innate source of IL-17 and IL-22. J Exp Med. 2009;206(1):35-41. DOI: http://dx.doi.org/10.1084/jem.20072713
Guo X, Liang Y, Zhang Y, Lasorella A, Kee BL, Fu YX. Innate lymphoid cells control early colonization resistance against Intestinal pathogens through ID2-dependent regulation of the microbiota. Immunity. 2015;42(4):731-743. DOI: http://dx.doi.org/10.1016/j.immuni.2015.03.012
Hepworth MR, Monticelli LA, Fung TC, Ziegler CG, Grunberg S, Sinha R, et al. Innate lymphoid cells regulate CD4+ T-cell responses to intestinal commensal bacteria. Nature. 2013;498(7452):113-117. DOI: http://dx.doi.org/10.1038/nature12240
Hepworth MR, Fung TC, Masur SH, Kelsen JR, McConnell FM, Dubrot J, et al. Immune tolerance. Group 3 innate lymphoid cells mediate intestinal selection of commensal bacteria-specific CD4(+) T cells. Science. 2015;348(6238):1031-1035. DOI: http://dx.doi.org/10.1126/science.aaa4812
Farkas AM, Ivanov, II. Escaping negative selection: ILC you in the gut. Immunity. 2015;43(1):12-14. DOI: http://dx.doi.org/10.1016/j.immuni.2015.07.006
Xu H, Wang X, Liu DX, Moroney-Rasmussen T, Lackner AA, Veazey RS. IL-17-producing innate lymphoid cells are restricted to mucosal tissues and are depleted in SIV-infected macaques. Mucosal Immunol. 2012;5(6):658-669. DOI: http://dx.doi.org/10.1038/mi.2012.39
Sanos SL, Bui VL, Mortha A, Oberle K, Heners C, Johner C, et al. RORgammat and commensal microflora are required for the differentiation of mucosal interleukin 22-producing NKp46+ cells. Nat Immunol. 2009;10(1):83-91. DOI: http://dx.doi.org/10.1038/ni.1684
Sonnenberg GF, Artis D. Innate lymphoid cell interactions with microbiota: Implications for intestinal health and disease. Immunity. 2012;37(4):601-610. DOI: http://dx.doi.org/10.1016/j.immuni.2012.10.003
Mielke LA, Jones SA, Raverdeau M, Higgs R, Stefanska A, Groom JR, et al. Retinoic acid expression associates with enhanced IL-22 production by gammadelta T cells and innate lymphoid cells and attenuation of intestinal inflammation. J Exp Med. 2013;210(6):1117-1124. DOI: http://dx.doi.org/10.1084/jem.20121588
Buonocore S, Ahern PP, Uhlig HH, Ivanov II, Littman DR, Maloy KJ, et al. Innate lymphoid cells drive interleukin-23-dependent innate intestinal pathology. Nature. 2010;464(7293):1371-1375. DOI: http://dx.doi.org/10.1038/nature08949
Van Maele L, Carnoy C, Cayet D, Ivanov S, Porte R, Deruy E, et al. Activation of Type 3 innate lymphoid cells and interleukin 22 secretion in the lungs during streptococcus pneumoniae infection. J Infect Dis. 2014;210(3):493-503. DOI: http://dx.doi.org/10.1093/infdis/jiu106
Klose CS, Kiss EA, Schwierzeck V, Ebert K, Hoyler T, D’Hargues Y, et al. A T-bet gradient controls the fate and function of CCR6-RORgammat+ innate lymphoid cells. Nature. 2013;494(7436):261-265. DOI: http://dx.doi.org/10.1038/nature11813
Colonna M. Immunology: An innate regulatory cell. Nature. 2013;498(7452):42-43. DOI: http://dx.doi.org/10.1038/498042a
Walker JA, Barlow JL, McKenzie AN. Innate lymphoid cells. How did we miss them. Nat Rev Immunol. 2013;13(2):75-87. DOI: http://dx.doi.org/10.1038/nri3349
Neill DR, McKenzie AN. Nuocytes and beyond: new insights into helminth expulsion. Trends Parasitol. 2011;27(5):214-221. DOI: http://dx.doi.org/10.1016/j.pt.2011.01.001
Maizels RM, Hewitson JP, Smith KA. Susceptibility and immunity to helminth parasites. Curr Opin Immunol. 2012;24(4):459-466. DOI: http://dx.doi.org/10.1016/j.coi.2012.06.003
Artis D, Wang ML, Keilbaugh SA, He W, Brenes M, Swain GP, et al. RELMbeta/FIZZ2 is a goblet cell-specific immune-effector molecule in the gastrointestinal tract. Proc Natl Acad Sci U S A. 2004;101(37):13596-13600. DOI: http://dx.doi.org/10.1073/pnas.0404034101
Maizels RM, Withers DR. MHC-II: a mutual support system for ILCs and T cells. Immunity. 2014;41(2):174-176. DOI: http://dx.doi.org/10.1016/j.immuni.2014.07.006
Boyd A, Ribeiro JM, Nutman TB. Human CD117 (cKit)+ innate lymphoid cells have a discrete transcriptional profile at homeostasis and are expanded during filarial infection. PLoS One. 2014;9(9):e108649. DOI: http://dx.doi.org/10.1371/journal.pone.0108649
Gladiator A, Wangler N, Trautwein-Weidner K, LeibundGut-Landmann S, et al. Cutting edge: IL-17-secreting innate lymphoid cells are essential for host defense against fungal infection. J Immunol. 2013;190(2):521-525. DOI: http://dx.doi.org/10.4049/jimmunol.1202924
Valero A, Quirce S, Dávila I, Delgado J, Domínguez-Ortega J. Allergic respiratory disease: different allergens, different symptoms. Allergy. 2017;72(9):1306-1316. DOI: http://dx.doi.org/10.1111/all.13141
Sonnenberg GF, Artis D. Innate lymphoid cells in the initiation, regulation and resolution of inflammation. Nat Med. 2015;21(7):698-708. DOI: http://dx.doi.org/10.1038/nm.3892
Bartemes KR, Iijima K, Kobayashi T, Kephart GM, McKenzie AN, Kita H. IL-33-responsive lineage- CD25+ CD44(hi) lymphoid cells mediate innate type 2 immunity and allergic inflammation in the lungs. J Immunol. 2012;188(3):1503-1513. DOI: http://dx.doi.org/10.4049/jimmunol.1102832
Chang YJ, Kim HY, Albacker LA, Baumgarth N, McKenzie AN, Smith DE, et al. Innate lymphoid cells mediate influenza-induced airway hyper-reactivity independently of adaptive immunity. Nat Immunol. 2011;12(7):631-638. DOI: http://dx.doi.org/10.1038/ni.2045
Li H, Richert-Spuhler LE, Evans TI, Gillis J, Connole M, Estes JD, et al. Hypercytotoxicity and rapid loss of NKp44+ innate lymphoid cells during acute SIV infection. PLoS Pathog. 2014;10(12):e1004551. DOI: http://dx.doi.org/10.1371/journal.ppat.1004551
Mudd JC, Brenchley JM. ILC you later: Early and irreparable loss of innate lymphocytes in HIV infection. Immunity. 2016;44(2):216-218. DOI: http://dx.doi.org/10.1016/j.immuni.2016.01.022
Klose CS, Artis D. Innate lymphoid cells as regulators of immunity, inflammation and tissue homeostasis. Nat Immunol. 2016;17(7):765-774. DOI: http://dx.doi.org/10.1038/ni.3489
Russell SE, Walsh PT. Sterile inflammation - do innate lymphoid cell subsets play a role. Front Immunol. 2012;3:246. DOI: http://dx.doi.org/10.3389/fimmu.2012.00246
Cording S, Medvedovic J, Aychek T, Eberl G. Innate lymphoid cells in defense, immunopathology and immunotherapy. Nat Immunol. 2016;17(7):755-757. DOI: http://dx.doi.org/10.1038/ni.3448
Brestoff JR, Kim BS, Saenz SA, Stine RR, Monticelli LA, Sonnenberg GF, et al. Group 2 innate lymphoid cells promote beiging of white adipose tissue and limit obesity. Nature. 2015;519(7542):242-246. DOI: http://dx.doi.org/10.1038/nature14115
Flach M, Diefenbach A. Adipose tissue: ILC-2 crank up the heat. Cell Metab. 2015;21(2):152-153. DOI: http://dx.doi.org/10.1016/j.cmet.2015.01.015
Molofsky AB, Nussbaum JC, Liang HE, Van Dyken SJ, Cheng LE, Mohapatra A, et al. Innate lymphoid type 2 cells sustain visceral adipose tissue eosinophils and alternatively activated macrophages. J Exp Med. 2013;210(3):535-549. DOI: http://dx.doi.org/10.1084/jem.20121964
Marchesi JR, Adams DH, Fava F, Hermes GDA, Hirschfield GM, Hold G, et al. The gut microbiota and host health: A new clinical frontier. Gut. 2016;65(2):330-339. DOI: http://dx.doi.org/10.1136/gutjnl-2015-309990
Powell N, Lo JW, Biancheri P, Vossenkämper A, Pantazi E, Walker AW, et al. Interleukin 6 increases production of cytokines by colonic innate lymphoid cells in mice and patients with chronic intestinal inflammation. Gastroenterology. 2015;149(2):456-467.e15. DOI: http://dx.doi.org/10.1053/j.gastro.2015.04.017
Van-Der-Gracht E, Zahner S, Kronenberg M. When insult is added to injury: Cross talk between ILCs and intestinal epithelium in IBD. Mediators Inflamm. 2016;2016:9765238. DOI: http://dx.doi.org/10.1155/2016/9765238.
Park CO, Noh S, Jin S, Lee NR, Lee YS, Lee H, et al. Insight into newly discovered innate immune modulation in atopic dermatitis. Exp Dermatol. 2013;22(1):6-9. DOI: http://dx.doi.org/10.1111/exd.12034
Salimi M, Barlow JL, Saunders SP, Xue L, Gutowska-Owsiak D, Wang X, et al. A role for IL-25 and IL-33-driven type-2 innate lymphoid cells in atopic dermatitis. J Exp Med. 2013;210(13):2939-2950. DOI: http://dx.doi.org/10.1084/jem.20130351
Pantelyushin S, Haak S, Ingold B, Kulig P, Heppner FL, Navarini AA, et al. Rorgammat+ innate lymphocytes and gammadelta T cells initiate psoriasiform plaque formation in mice. J Clin Invest. 2012;122(6):2252-2256. DOI: http://dx.doi.org/10.1172/JCI61862
Pasparakis M, Haase I, Nestle FO. Mechanisms regulating skin immunity and inflammation. Nat Rev Immunol. 2014;14(5):289-301. DOI: http://dx.doi.org/10.1038/nri3646
Villanova F, Flutter B, Tosi I, Grys K, Sreeneebus H, Perera GK, et al. Characterization of innate lymphoid cells in human skin and blood demonstrates increase of NKp44+ ILC-3 in psoriasis. J Invest Dermatol. 2014;134(4):984-991. DOI: http://dx.doi.org/10.1038/jid.2013.477
Vargas-Becerra MH. Fisiopatología del asma. Neumol Cir Torax. 2009;68(2):111-115. Disponible en: http://www.medigraphic.com/pdfs/neumo/nt-2009/nts092e.pdf
Matsuoka T, Shamji MH, Durham SR. Allergen immunotherapy and tolerance. Allergol Int. 2013;62(4):403-413. DOI: http://dx.doi.org/10.2332/allergolint.13-RAI-0650
Chang YJ, DeKruyff RH, Umetsu DT. The role of type 2 innate lymphoid cells in asthma. J Leukoc Biol. 2013;94(5):933-940. DOI: http://dx.doi.org/10.1189/jlb.0313127
Cheng H, Jin C, Wu J, Zhu S, Liu YJ, Chen J. Guards at the gate: Physiological and pathological roles of tissue-resident innate lymphoid cells in the lung. Protein Cell. 2017. DOI: http://dx.doi.org/10.1007/s13238-017-0379-5
Moffatt MF, Gut IG, Demenais F, Strachan DP, Bouzigon E, Heath S, et al. A large-scale, consortium-based genomewide association study of asthma. N Engl J Med. 2010;363(13):1211-1221. DOI: http://dx.doi.org/10.1056/NEJMoa0906312
Kim HY, Chang YJ, Subramanian S, Lee HH, Albacker LA, Matangkasombut P, et al. Innate lymphoid cells responding to IL-33 mediate airway hyperreactivity independently of adaptive immunity. J Allergy Clin Immunol. 2012;129(1):216-227. e1-6. DOI: http://dx.doi.org/10.1016/j.jaci.2011.10.036
Deckers J, Branco Madeira F, Hammad H. Innate immune cells in asthma. Trends Immunol. 2013;34(11):540-547. DOI: http://dx.doi.org/10.1016/j.it.2013.08.004
Halim TY, Krauss RH, Sun AC, Takei F. Lung natural helper cells are a critical source of Th2 cell-type cytokines in protease allergen-induced airway inflammation. Immunity. 2012;36(3):451-463. DOI: http://dx.doi.org/10.1016/j.immuni.2011.12.020
Wilhelm C, Hirota K, Stieglitz B, Van-Snick J, Tolaini M, Lahl K, et al. An IL-9 fate reporter demonstrates the induction of an innate IL-9 response in lung inflammation. Nat Immunol. 2011;12(11):1071-1077. DOI: http://dx.doi.org/10.1038/ni.2133
Klein-Wolterink RG, Kleinjan A, Van-Nimwegen M, Bergen I, De-Bruijn M, Levani Y, et al. Pulmonary innate lymphoid cells are major producers of IL-5 and IL-13 in murine models of allergic asthma. Eur J Immunol. 2012;42(5):1106-1116. DOI: http://dx.doi.org/10.1002/eji.201142018
Kim BS, Wojno ED, Artis D. Innate lymphoid cells and allergic inflammation. Curr Opin Immunol. 2013;25(6):738-744. DOI: http://dx.doi.org/10.1016/j.coi.2013.07.013
Holtzman MJ, Byers DE, Alexander-Brett J, Wang X. The role of airway epithelial cells and innate immune cells in chronic respiratory disease. Nat Rev Immunol. 2014;14(10):686-698. DOI: http://dx.doi.org/10.1038/nri3739
Martinez-Gonzalez I, Mathä L, Steer CA, Takei F. Immunological memory of group 2 innate lymphoid cells. Trends Immunol. 2017;38(6):423-431. DOI: http://dx.doi.org/10.1016/j.it.2017.03.005
Sutherland ER, Lehman EB, Teodorescu M, Wechsler ME. Body mass index and phenotype in subjects with mild-to-moderate persistent asthma. J Allergy Clin Immunol. 2009;123(6):1328-1334.e1. DOI: http://dx.doi.org/10.1016/j.jaci.2009.04.005
Kim HY, Lee HJ, Chang YJ, Pichavant M, Shore SA, Fitzgerald KA, et al. IL-17 producing innate lymphoid cells and the NLRP3 inflammasome facilitate obesity-associated airway hyperreactivity. Nat Med. 2014;20(1):54-61. DOI: http://dx.doi.org/10.1038/nm.3423
Hulse KE. Immune mechanisms of chronic rhinosinusitis. Curr Allergy Asthma Rep. 2016;16(1):1. DOI: http://dx.doi.org/10.1007/s11882-015-0579-0
Zuo J, Shan Z, Zhou L, Yu J, Liu X, Gao Y. Increased CD160 expression on circulating natural killer cells in atherogenesis. J Transl Med. 2015;13:188. DOI: http://dx.doi.org/10.1186/s12967-015-0564-3
Engelbertsen D, Foks AC, Alberts-Grill N, Kuperwaser F, Chen T, Lederer JA, et al. Expansion of CD25+ innate lymphoid cells reduces atherosclerosis. Arterioscler Thromb Vasc Biol. 2015;35(12):2526-2535. DOI: http://dx.doi.org/10.1161/ATVBAHA.115.306048
Mattner J, Wirtz S. Friend or foe? The ambiguous role of innate lymphoid cells in cancer development. Trends Immunol. 2017;38(1):29-38. DOI: http://dx.doi.org/10.1016/j.it.2016.10.004
Li J, Razumilava N, Gores GJ, Walters S, Mizuochi T, Mourya R, et al. Biliary repair and carcinogenesis are mediated by IL-33-dependent cholangiocyte proliferation. J Clin Invest. 2014;124(7):3241-3251. DOI: http://dx.doi.org/10.1172/JCI73742
Jovanovic IP, Pejnovic NN, Radosavljevic GD, Pantic JM, Milovanovic MZ, Arsenijevic NN, et al. Interleukin-33/ST2 axis promotes breast cancer growth and metastases by facilitating intratumoral accumulation of immunosuppressive and innate lymphoid cells. Int J Cancer. 2014;134(7):1669-1682. DOI: http://dx.doi.org/10.1002/ijc.28481
Chan IH, Jain R, Tessmer MS, Gorman D, Mangadu R, Sathe M, et al. Interleukin-23 is sufficient to induce rapid de novo gut tumorigenesis, independent of carcinogens, through activation of innate lymphoid cells. Mucosal Immunol. 2014;7(4):842-856. DOI: http://dx.doi.org/10.1038/mi.2013.101
Carrega P, Campana S, Bonaccorsi I, Ferlazzo G. The yin and yang of innate lymphoid cells in cancer. Immunol Lett. 2016;179:29-35. DOI: http://dx.doi.org/10.1016/j.imlet.2016.06.003
Gowans JL. The recirculation of lymphocytes from blood to lymph in the rat. J Physiol. 1959;146(1):54-69. DOI: http://dx.doi.org/10.1113/jphysiol.1959.sp006177
Reinherz EL, Kung PC, Breard JM, Goldstein G, Schlossman SF. T cell requirements for generation of helper factor(s) in man: Analysis of the subsets involved. J Immunol. 1980;124(4):1883-1887.
Nomenclature for clusters of differentiation (CD) of antigens defined on human leukocyte populations. IUIS-WHO Nomenclature Subcommittee. Bull World Health Organ. 1984;62(5):809-815. Disponible en: https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2536217/
Bernard A, Boumsell L. The clusters of differentiation (CD) defined by the First International Workshop on Human Leucocyte Differentiation Antigens. Hum Immunol. 1984;11(1):1-10. DOI: http://dx.doi.org/10.1016/0198-8859(84)90051-X
Mosmann TR, Coffman RL. Two types of mouse helper T-cell clone implications for immune regulation. Immunol Today. 1987;8(7-8):223-227. DOI: http://dx.doi.org/10.1016/0167-5699(87)90171-X

Esta obra está bajo una licencia internacional Creative Commons Atribución-NoComercial 4.0.
Derechos de autor 2017 Revista Alergia México