Foreword: The neuroimmune biology of growth and lactogenic hormones

NeuroImmune Biology

Volumn 2, Issue C, 2002, Pages

[No Author Info available]

Author keywords

[No Author keywords available]

Indexed keywords

EID: 77957099383     PISSN: 15677443     EISSN: None     Source Type: Book Series    
DOI: 10.1016/S1567-7443(02)80001-1     Document Type: Editorial

References (65)

1. Selye H. Stress and disease. Science 122 (1955) 625-631
2. Berczi I. The effect of growth hormone and related hormones on the immune system. In: Berczi I. (Ed). Pituitary Function and Immunity (1986), CRC Press, Boca Raton, FL 133-159
3. Rapaport R. Growth hormone therapy and immune function. In: Berczi I., and Gorczynsky R. (Eds). New foundation of Biology. NeuroImmune Biology Vol. 1 (2001), Elsevier 403-408
4. Nagy E., and Berczi I. Immunodeficiency in hypophysectomized rats. Acta Endocrinol 89 (1978) 530-537
5. Nagy E., and Berczi I. Prolactin and contact sensitivity. Allergy 36 (1981) 429-431
6. Berczi I., Nagy E., Kovacs K., and Horvath E. Regulation of humoral immunity in rats by pituitary hormones. Acta Endocrinol 98 (1981) 506-513
7. Nagy E., Berczi I., and Friesen H.G. Regulation of immunity in rats by lactogenic and growth hormones. Acta Endocrinol 102 (1983) 351-357
8. Berczi I., Nagy E., Asa S.L., and Kovacs K. Pituitary hormones and contact sensitivity in rats. Allergy 38 (1983) 325-330
9. Nagy E., Berczi I., Wren G.E., Asa S.L., and Kovacs K. Immunomodulation by bromocriptine. Immunopharmacology 6 (1983) 231-243
10. Nagy E., and Berczi I. Pituitary dependence of bone marrow function. Brit J Haematol 71 (1989) 457-462
11. Berczi I., Nagy E., Asa S.L., and Kovacs K. The influence of pituitary hormones on adjuvant arthritis. Arthritis Rheum 27 (1984) 682-688
12. Nagy E., and Berczi I. Immunomodulation by tamoxifen and pergolide. Immunopharmacology 12 (1986) 145-153
13. Berczi I., and Nagy E. Placental lactogen is a hemopoietic hormone. Brit J Haematol 79 (1991) 355-358
14. (in press). Berczi I., and Szentivanyi A. Growth and lactogenic hormones, insulin-like growth factor, insulin. In: Szentivanyi A., and Berczi I. (Eds). The Immune-Neuroendocrine Circuitry, Neuroimmune Biology Vol. 3 (2002), Elsevier
15. Soares M.J. Uteroplacental prolactin family: Immunological regulators of viviparity. In: Matera L., and Rapaport R. (Eds). Growth and Lactogenic Hormones. Neuroimmune Biology Vol. 2 (2002), Elsevier 187-202
16. Kaplan S.L., Grumbach M.M., Friesen H.G., and Costom B.H. Thyrotropin-releasing factor (TRF) effect on secretion of human pituitary prolactin and thyrotropin in children and in idiopathic hypopituitary dwarfism: further evidence for hypophysiotropic hormone deficiencies. J Clinical Endocrinology & Metabolism 35 (1972) 825-830
17. Sinha Y.N., Salocks C.B., and Vanderlaan W.P. Pituitary and serum concentrations of prolactin and GH in Snell dwarf mice. Proc Soc Exp Biol Med 150 1 (1975 Oct) 207-210
18. Barkley M.S., Bartke A., Gross D.S., and Sinha Y.N. Prolactin status of hereditary dwarf mice. Endocrinology 110 6 (1982 Jun) 2088-2096
19. Soares M.J., Bartke A., Colosi P., and Talamantes F. Identification of a placental lactogen in pregnant Snell and Ames dwarf mice. Proc Soc Exp Biol Med 175 1 (1984 Jan) 106-108
20. Pfaffle R.W., Blankenstein O., Wuller S., and Kentrup H. Combined pituitary hormone deficiency: role of Pit-1 and Prop-1. Acta Paediatr Suppl 88 433 (1999 Dec) 33-41
21. Gala R.R. The influence of thyroxine, growth hormone and prolactin alone and in combination on the production of prolactin-like activity by splenocytes from Snell dwarf mice. Life Sci 57 2 (1995) 113-122
22. Nagy E., and Berczi I. Hypophysectomized rats depend on residual prolactin for survival. Endocrinology 146 (1991) 2776-2784
23. Horseman N.D., Zhao W., Montecino-Rodrigez E., Tanaka M., Nakashima K., Engle S.J., Smith F., Markoff E., and Dorshkind K. Defective mammopoiesis, but normal hematopoiesis, in mice with a targeted disruption of the prolactin gene. EMBO J 16 (1997) 6926-6935
24. Bole-Feysot C., Goffin V., Edery M., Binart N., and Kelly P.A. Prolactin (PRL) and its receptor: Actions, signal transduction pathways and phenotypes observed in PRL-receptor knockout mice. Endocrine Rev 19 (1998) 225-268
25. Dorshkind K., and Horseman N.D. The roles of prolactin, growth hormone, insulin-like growth factor-I, and Thyroid hormones in lymphocyte development and function. Insights from genetic models of hormone and hormone receptor deficiency. Endocrine Rev 21 (2000) 292-312
26. Berczi I. Neuroimmune Biology-An introduction. In: Berczi I., and Gorczynski R. (Eds). New Foundation of Biology. Neuroimmune Biology Series Vol. 1 (2001), Elsevier 3-45
27. th edition (1999), Lippincott-Raven, New York 741-774
28. Notarangelo L.D., Gilliani S., Mazza C., Mella P., Savoldi G., Rodriguez-Perez C., Mazzolari E., Fiorini M., Duse M., Plebani A., Ugazio A.G., Vihinen M., Candotti F., and Schumacher R.F. Of genes and phenotypes: the immunological and molecular spectrum of combined immune deficiency. Defects of the gamma (c)-JAK3 signaling pathway as a model. Immunol Rev 178 (2000) 39-48
29. Freeman M.E., Kanyicska B., Lerant A., and Nagy G. Prolactin: structure, function, and regulation of secretion. Physiol Rev 80 (2000) 1523-1631
30. Ivashkiv L.B. Jak-STAT signaling pathways in cells of the immune system. Rev Immunogenet 2 (2000) 220-230
31. Berczi I. The role of the growth and lactogenic hormone family in immune function. Neuroimmunomodulation 1 (1994) 201-216
32. Berczi I., and Szentivanyi A. Immunocompetence. In: Berczi I., and Szentivanyi A. (Eds). The Immune-Neuroendocrine Circuitry. Neuroimmune Biology Vol. 2 (2002), Elsevier
33. Baines M.G. Olfactory stimuli and allo-recognition. In: Berczi I., and Gorczynski R. (Eds). New Foundation of Biology, Neuroimmune Biology Vol. 1 (2001), Elsevier 313-329
34. Choudhury SR, Knapp LA. Human reproductive failure I: immunological factors. Hum Reprod Update 2001 Mar-Apr; 7(2): 113-134
35. Ellis L.A., Mastro A.M., and Picciano M.F. Do milk cytokines and hormones influence neonatal immune function?. J Nutr 127 (1997) 985S-988S
36. Korhonen H., Marnila P., and Gill H.S. Milk immunoglobulins and complement factors. Br J Nutr 84 Suppl 1 (2000) S75-S80
37. Weiss Carrington P. Secretory immunology of the mammary gland. In: Berczi I., and Kovacs K. (Eds). Hormones and Immunity (1987), MTP Press, Lancaster, UK 172-202
38. Takala J., Ruokonen E., Webster N.R., et al. Increased mortality associated with growth hormone treatment in critically ill adults. N Engl J Med 341 (1999) 785-792
39. Berczi I. Neurohormonal host defence in endotoxin shock. Ann NY Acad Sci 840 (1998) 787-802
40. Haeryfar S.M.M., and Berczi I. The thymus and the acute phase response. Cell Mol Biol 47 (2001) 145-156
41. Berczi I., Bertok L., and Chow D. Natural immunity and neuroimmune host defence. Ann NY Acad Sci 917 (2001) 248-257
42. Jeschke M.G., Herndon D.N., Wolf S.E., et al. Recombinant human growth hormone alters acute phase reactant proteins, cytokine expression, and liver morphology in burned rats. J Surg Res 83 (1999) 122-129
43. Derfalvi B., Igaz P., Fulop K.A., Szalai C., and Falus A. Interleukin-6-induced production of type II acute phase proteins and expression of junB gene are downregulated by human recombinant growth hormone in vitro. Cell Biol Int 24 (2000) 109-114
44. Berczi I. The influence of pituitary-adrenal axis on the immune system. In: Berczi I. (Ed). Pituitary Function and Immunity (1986), CRC Press, Boca Raton, FL 49-132
45. Berczi I., Nagy E., Matusik R.J., and Friesen H.G. Pituitary hormones regulate c-myc and DNA synthesis in lymphoid tissue. J Immunol 146 (1991) 2201-2206
46. 3 pituitary adenoma cells can reverse thymic aging in rats. Proc Natl Acad Sci USA 83 (1986) 5663-5667
47. Berczi I. Immunoregulation by the pituitary gland. In: Berczi I. (Ed). Pituitatry Function and Immunity (1966), CRC Press, Boca Raton, CA
48. Montgomery D.W., Zukoski C.F., Shah G.N., Buckley A.R., Pacholczyk T., and Russell D.H. Concanavalin A-stimulated murine splenocytes produce a factor with prolactin-like bioactivity and immunoreactivity. Biochem Biophys Res Commun 145 (1987) 692-698
49. Hartmann D.P., Holaday J.W., and Bernton D.W. Inhibition of lymphocyte proliferation by antibodies to prolactin. FASEB J 3 (1989) 2194-2202
50. Clevenger C.V., Russell D.H., Appasamy P.M., and Prystowsky M.B. Regulation of interleukin-2 driven T-lymphocyte proliferation by prolactin. Proc Natl Acad Sci USA 87 (1990) 6460-6464
51. (this volume). Weigent D. Growth hormone and insulin-like growth factor-1 production by cells of the immune system. In: Matera L., and Rapaport R. (Eds). Growth and Lactogenic Hormones. Neuroimmune Biology Vol. 2 (2002), Elsevier 87-100
52. Hooghe E. Signal transduction and modulation of gene expression by prolactin in human, leukocites. In: Matera L., and Rapaport R. (Eds). Growth and Lactogenic Hormones. Neuroimmune Biology Vol. 2 (2002), Elsevier 123-136
53. Sabharwal P., Glaser R., Lafuse W., Varma S., Liu Q., Arkins S., Kooijman R., Kutz L., Kelley K.W., and Malarkey W.B. Prolactin synthesized and secreted by human peripheral blood mononuclear cells: an autocrine growth factor for lymphoproliferation. Proc Natl Acad Sci USA 89 (1992) 7713-7716
54. Handwerger S., and Freemark M. The roles of placental growth hormone and placental lactogen in the regulation of human fetal growth and development. J Pediatr Endocrinol Metab 13 (2000) 343-356
55. DiMattia G.E., Gellersen B., Duckworth M.L., and Friesen H.G. Human prolactin gene expression: The use of an alternative noncoding exon in decidua and the IM-9_P3 lymphoblastoid cell line. J Biol Chem 265 (1990) 16412-16421
56. Delhase M., Vergani P., Malur A., Hooghe Peters E.L., and Hooghe R.J. The transcription factor Pit-1/HGF-1 is expressed in hematopoietic and lymphoid tissues. Eur J Immunol 23 (1993) 951-955
57. Fearon D.T., Manders P., and Wagner S.D. Arrested differentiation, the self-renewing memory lymphocyte, and vaccination. Science 293 5528 (2001 Jul 13) 248-250
58. Sprent J., and Tough D.F. T cell death and memory. Science 293 5528 (2001 Jul 13) 245-248
59. Nayak R., Mitra-Kaushik S., and Shaila M.S. Perpetuation of immunological memory: a relay hypothesis. Immunology 102 4 (2001 Apr) 387-395
60. Ashton-Rickardta P.G., and Opferman J.T. Memory T lymphocytes. Cell Mol Life Sci 56 1-2 (1999 Oct 1) 69-77
61. Sprent J., and Surh C.D. Generation and maintenance of memory T cells. Curr Opin Immunol 13 2 (2001 Apr) 248-254
62. Akbar A.N., Lord J.M., and Salmon M. IFN-alpha and IFN-beta: a link between immune memory and chronic inflammation. Immunol Today 21 7 (2000 Jul) 337-342
63. Cho B.K., Rao V.P., Ge Q., Eisen H.N., and Chen J. Homeostasis-stimulated proliferation drives naive T cells to differentiate directly into memory T cells. J Exp Med 192 4 (2000 Aug 21) 549-556
64. Claman H.N. Corticosteroids-immunologic and anti-inflammatory effects. In: Berczi I., and Kovacs K. (Eds). Hormones and Immunity (1987), MTP Press, Lancaster, UK 38-42
65. In: Berczi I., and Szentivanyi A. (Eds). The Immune-Neuroendocrine Circuitry. Neuroimmune Biology Vol. 3 (2002), Elsevier