The Journal of Allergy and Clinical Immunology
Volume 125, Issue 2, Supplement 2 , Pages S53-S72, February 2010

Immunologic messenger molecules: Cytokines, interferons, and chemokines

  • Scott P. Commins, MD, PhD
  • ,
  • Larry Borish, MD

      Affiliations

    • Corresponding Author InformationReprint requests: Larry Borish, MD, University of Virginia Health System, Asthma and Allergic Disease Center, Box 801355, Charlottesville, VA 22908-1355.
  • ,
  • John W. Steinke, PhD

University of Virginia Health System, Carter Center for Immunology Research, Asthma and Allergic Disease Center, Charlottesville, Va

Received 15 June 2009; received in revised form 9 July 2009; accepted 10 July 2009. published online 25 November 2009.

Cytokines and chemokines are secreted proteins involved in numerous aspects of cell growth, differentiation, and activation. A prominent feature of these molecules is their effect on the immune system with regard to cell trafficking and development of immune tissue and organs. The nature of an immune response determines which cytokines are produced and ultimately whether the response is cytotoxic, humoral, cell mediated, or allergic. For this chapter, cytokines are grouped according to those that are predominantly antigen-presenting cell or T lymphocyte derived; that mediate cytotoxic, humoral, cell mediated, and allergic immunity; or that are immunosuppressive. A discussion of chemokine function and their role in cell trafficking and disease follows.

Key words: Cytokine, chemokine, interferon, antigen-presenting cell, T lymphocyte

Abbreviations used: ABPA, Allergic bronchopulmonary aspergillosis, AHR, Airway hyperreactivity, APC, Antigen-presenting cell, APRIL, A proliferation-inducing signal, BAFF, B-cell activation factor from the TNF family, DC, Dendritic cell, Foxp3, Forkhead box protein 3, gp130, Glycoprotein 130, ICAM, Intercellular adhesion molecule, IFNGR, IFN-γ receptor, IL-1ra, IL-1 receptor antagonist, IL-2R, IL-2 receptor, IL-4R, IL-4 receptor, IL-5R, IL-5 receptor, IL-6R, IL-6 receptor, IL-10R, IL-10 receptor, IL-12R, IL-12 receptor, IL-13R, IL-13 receptor, IL-17R, IL-17 receptor, IL-20R, IL-20 receptor, IL-22R, IL-22 receptor, IRS, Insulin response element, iTreg, Induced regulatory T, JAK, Janus kinase, MAPK, Mitogen-activated protein kinase, MCP, Monocyte chemoattractant protein, M-CSF, Macrophage colony-stimulating factor, MIP, Macrophage inflammatory protein, NK, Natural killer, nTreg, Natural regulatory T, ROR, Retinoic acid receptor–related orphan receptor, SCF, Stem cell factor, STAT, Signal transducer and activator of transcription, TACI, Transmembrane activator and calcium modulator and cyclophilin ligand interactor, T-bet, T-box expressed in T cells, Treg, Regulatory T, TSLP, Thymic stromal lymphopoietin, VCAM, Vascular cell adhesion molecule

 

 Supported by National Institutes of Health grant R01 AI-057438 and AI-50989 (L.B. and J.W.S.), and by an American Academy of Allergy, Asthma & Immunology/GlaxoSmithKline career development award and T32 AI-007496-14 (S.P.C.).

 Disclosure of potential conflict S. P. Commins has received research support from GlaxoSmithKline. L. Borish has received research support from Merck and Genentech. J. W. Steinke has received research support from the National Institutes of Health.

PII: S0091-6749(09)01075-6

doi:10.1016/j.jaci.2009.07.008

Refers to article:

  • Immunologic messenger molecules: Cytokines, interferons, and chemokines

    The Journal of Allergy and Clinical Immunology February 2010 (Vol. 125, Issue 2, Supplement 2, Page S349)

The Journal of Allergy and Clinical Immunology
Volume 125, Issue 2, Supplement 2 , Pages S53-S72, February 2010