Literature DB >> 7489335

The role of the growth and lactogenic hormone family in immune function.

I Berczi1.   

Abstract

The influence of various members of the growth and lactogenic hormone family on the immune system is reviewed. A general hypothesis is proposed for growth control in higher animals. It is suggested that immune reactions, which are based on lymphocyte proliferation, obey the general rules of growth control in vertebrate animals. Growth and lactogenic hormones (GLH) are required for the development and function of the immune system and are suggested to deliver the first signal that prepares the cell for proliferation, differentiation and function. This signal has already been designated by other as the competence signal which initiates the cell cycle. Second signals are delivered through the antigen receptor, and/or by some other cell surface receptors (adhesion molecules) and always involve cell-to-cell ('bridging') and/or cell-to-matrix interaction. This category of signals is designated as stromal or adherence signals. The lymphocyte adhesion molecules that mediate second signals have evolved form organ- and tissue-specific recognition/regulatory molecules. The antigen receptors have been perfected during evolution from self recognition to specific-antigen recognition. Apart from this exquisitely specific mechanism of immune recognition, there is evidence for other less specific means of recognition by adherence molecules that mediate the activation of the immune system during nonspecific injury and also play a role in the elimination of degenerated and neoplastic cells. Signals delivered through adhesion molecules have the power to commit the cell to a given activity which is executed by the delivery of third signals in the form of soluble cytokines, usually, but not always, by the same cell delivering the second signal(s). The combination of these three groups of signals will ultimately determine whether or not the cell will proliferate, differentiate, maintain function or, perhaps, be committed to apoptosis. Therefore, GLH maintain immunocompetence which enables the immune system to respond to specific antigenic and tissue-derived stimuli in a self-regulated fashion. The adrenocorticotropic hormone-adrenal axis antagonizes the immunostimulatory effect of GLH. This basic pattern of lymphocyte regulation is influenced further by additional hormones, neurotransmitters and neuropeptides, mostly by the modulation of signal delivery. The constant interaction of neuroendocrine and internal immunoregulatory mechanisms assures the fine tuning of the immune system, so that it is able to function in homeostasis and harmony with the organism.

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Year:  1994        PMID: 7489335     DOI: 10.1159/000097168

Source DB:  PubMed          Journal:  Neuroimmunomodulation        ISSN: 1021-7401            Impact factor:   2.492


  10 in total

1.  Chronic stress down-regulates growth hormone gene expression in peripheral blood mononuclear cells of older adults.

Authors:  W B Malarkey; H Wu; J T Cacioppo; K L Malarkey; K M Poehlmann; R Glaser; J K Kiecolt-Glaser
Journal:  Endocrine       Date:  1996-08       Impact factor: 3.633

Review 2.  Pituitary function during severe and life-threatening illnesses.

Authors:  C Gauna; G H van den Berghe; A J van der Lely
Journal:  Pituitary       Date:  2005       Impact factor: 4.107

Review 3.  Neuroimmune mechanisms in health and disease: 1. Health.

Authors:  H Anisman; M G Baines; I Berczi; C N Bernstein; M G Blennerhassett; R M Gorczynski; A H Greenberg; F T Kisil; R D Mathison; E Nagy; D M Nance; M H Perdue; D K Pomerantz; E R Sabbadini; A Stanisz; R J Warrington
Journal:  CMAJ       Date:  1996-10-01       Impact factor: 8.262

Review 4.  Neuroimmune mechanisms in health and disease: 2. Disease.

Authors:  H Anisman; M G Baines; I Berczi; C N Bernstein; M G Blennerhassett; R M Gorczynski; A H Greenberg; F T Kisil; R D Mathison; E Nagy; D M Nance; M H Perdue; D K Pomerantz; E R Sabbadini; A Stanisz; R J Warrington
Journal:  CMAJ       Date:  1996-10-15       Impact factor: 8.262

5.  The effect of prolactin (PRL) on the growth of Toxoplasma gondii tachyzoites in vitro.

Authors:  Katarzyna Dzitko; Justyna Gatkowska; Przemysław Płociński; Bozena Dziadek; Henryka Długońska
Journal:  Parasitol Res       Date:  2010-04-16       Impact factor: 2.289

6.  Adenohypophysitis in rat pituitary allografts.

Authors:  Fabio Rotondo; Andres Quintanar-Stephano; Sylvia L Asa; Matilde Lombardero; Istvan Berczi; Bernd W Scheithauer; Eva Horvath; Kalman Kovacs
Journal:  Int J Exp Pathol       Date:  2010-10       Impact factor: 1.925

Review 7.  Role of salsolinol in the regulation of pituitary prolactin and peripheral dopamine release.

Authors:  Márk Oláh; Ibolya Bodnár; Galit Daniel; Béla E Tóth; Miklós Vecsernyés; György M Nagy
Journal:  Reprod Med Biol       Date:  2011-05-03

8.  Differential effects of estrogen and medroxyprogesterone on basal and stress-induced growth hormone release, IGF-1 levels, and cellular immunity in postmenopausal women.

Authors:  W B Malarkey; M Burleson; J T Cacioppo; K Poehlmann; R Glaser; J K Kiecolt-Glaser
Journal:  Endocrine       Date:  1997-10       Impact factor: 3.633

9.  Failure of antibody response to polysaccharide antigen in treated panhypopituitary adults.

Authors:  A Mukherjee; M Helbert; W D J Ryder; R Borrow; J R E Davis; S M Shalet
Journal:  Clin Exp Immunol       Date:  2009-02-10       Impact factor: 4.330

10.  Effect of hyperprolactinaemia on Toxoplasma gondii prevalence in humans.

Authors:  Katarzyna Dzitko; Sebastian Malicki; Jan Komorowski
Journal:  Parasitol Res       Date:  2007-12-20       Impact factor: 2.289

  10 in total

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