Int J Sports Med 2000; 21(8): 602-607
DOI: 10.1055/s-2000-8477
Immunology
Georg Thieme Verlag Stuttgart ·New York

Comparison of Anti-Leukemic Immunity Against U937 Cells in Endurance Athletes Versus Sedentary Controls

J. Chiang1 , Y. W. Huang3 , M. L. Chen3 , S. Y. Wang4 , A. C. Huang1 , Y. J. Chen2, 5
  • 1 Graduate Institute of Sport Coaching Science, Chinese Culture University, Taipei, Taiwan, Republic of China
  • 2 Department of Martial Arts, Chinese Culture University, Taipei, Taiwan, Republic of China
  • 3 Department of Medical Research, Mackay Memorial Hospital, Taipei, Taiwan, Republic of China
  • 4 Department of Medical Research, Veterans General Hospital, Taipei, Taiwan, Republic of China
  • 5 Department of Radiation Oncology, Mackay Memorial Hospital, Taipei, Taiwan, Republic of China
Further Information

Publication History

Publication Date:
31 December 2000 (online)

To examine whether endurance athletes have higher anti-leukemic immunity than sedentary controls or not, we isolated peripheral blood mononuclear cells (MNC) from cyclists and sedentary controls to prepare conditioned media (CM) with various doses of phytohemagglutinin (PHA). The proliferation-inhibiting and differentiation-inducing activities of these PHA-MNC-CM on human leukemic U937 cells were investigated. Our results show that the growth inhibition activity of cyclists' PHA-MNC-CM were higher than that of controls. The dosage of PHA used to prepare MNC-CM to achieve about 90 % growth inhibition was 5 µg/ml in the control group and was 2 µg/ml in the athletes group. The differentiation-inducing effects were evaluated by morphological scoring, superoxide production, and monocyte-associated antigen expression (CD14 and CD68). These three parameters all demonstrated the differentiation-inducing effect of MNC-CM increased with increasing dose of PHA. These effects were significantly greater in the athletic when compared to the sedentary control group at all doses of PHA. The levels of TNF-α and IFN-γ in PHA-MNC-CM increased in a PHA dose-dependent manner and were much higher in the athletic group when compared to the controls. We conclude that the capacity of endurance athletes to activate anti-leukemic immunity is significantly higher than that of sedentary controls.

References

  • 1 Baehner R L, Nathan D G. Quantitative nitroblue tetrazolinum test in chronic granulomatous disease.  New Engl J Med. 1968;  278 971-976
  • 2 Baj Z, Kantorski J, Majewska E . et al . Immunological status of competitive cyclists before and after the training season.  Int J Sports Med. 1994;  15 319-324
  • 3 Ball E D, Guyre P M, Shen L, Maliszewski C R, Baker P E, Fanger M F. Gamma interferon induces monocytoid differentiation in the HL-60 cell line.  J Clin Invest. 1984;  74 1072-1077
  • 4 Bruce R A, Kasumi F, Hosmer D. Maximal oxygen intake and nomographic assessment of functional aerobic impairment in cardiovascular disease.  Am Heart J. 1973;  85 546-562
  • 5 Chen Y J, Shiao M S, Lee S S, Wang S Y. Effect of Cordyceps sinensis on the proliferation and differentiation of human leukemic U937 cells.  Life Sci. 1997;  60 2349-2359
  • 6 Fenton M J, Golenbock D T. LPS-binding proteins and receptors.  J Leuko Biol. 1998;  64 25-32
  • 7 Field C J, Gougeon R, Marliss E B. Circulating mononuclear cell numbers and function during intense exercise and recovery.  J Appl Physiol. 1991;  71 1089-1097
  • 8 Frisch R E, Wyshak G, Albright N L. Lower prevalence of breast cancer and cancers of the reproductive system among former college athletes compared to non-athletes.  Br J Cancer. 1985;  52 885-891
  • 9 Frisch R E, Wyshak G, Albright N L, Albright T E, Schiff I. Lower prevalance of non-reproductive system cancers among female former college athletes.  Med Sci Sports Exerc. 1989;  21 250-253
  • 10 Hickson R C, Bomze H A, Holloszy J O. Linear increase in aerobic power induced by a strenuous program of endurance exercise.  J Appl Physiol. 1977;  42 372-376
  • 11 Hoffman-Goetz L, Simpson J A, Cipp N, Arumugam Y, Houston M E. Lymphocyte subset responses to repeated submaximal exercise in men.  J Appl Physiol. 1990;  68 1069-1074
  • 12 Hoffman-Goetz L, Thorne R, Simpson J A, Arumugam Y. Exercise stress alters murine lymphocyte subset distribution in spleen, lymph node and thymus.  Clin Exp Immunol. 1989;  76 307-310
  • 13 Holness C L, Simmons D L. Molecular cloning of CD68, a human macrophage marker related to lysosomal glycoproteins.  Blood. 1993;  81 1607-1613
  • 14 Howley E T, Bassett D R, Welch H G. Criteria for maximal oxygen uptake: review and commentary.  Med Sci Sports Exerc. 1995;  27 1292-1301
  • 15 Lieu C W, Lee S S, Wang S Y. The effect of Ganoderma lucidum on induction of differentiation in leukemic U937 cells.  Anticancer Res. 1992;  12 1211-1215
  • 16 Lin Y S, Jan M S, Tsai T J, Chen H I. Immunomodulatory effects of acute exercise bout in sedentary and trained rats.  Med Sci Sports Exerc. 1995;  27 73-78
  • 17 Munker R, Koeffler P. In vitro action of tumor necrosis factor on myeloid leukemia cells.  Blood. 1987;  69 1102-1108
  • 18 Nieman D C, Berk L S, Simpson-Westerberg M . et al . Effects of long-endurance running on immune system parameters and lymphocyte function in experienced marathoners.  Int J Sports Med. 1989;  10 317-323
  • 19 Nieman D C, Buckley K S, Henson D A . et al . Immune function in marathon runners versus sedentary controls.  Med Sci Sports Exerc. 1995;  27 986-992
  • 20 Nieman D C, Henson D A, Gusewitch G . et al . Physical activity and immune function in elderly women.  Med Sci Sports Exerc. 1993;  25 823-831
  • 21 Onozaki K, Urawa H, Tamatani T . et al . Synergistic interactions of interleukin 1, interferon-beta, and tumor necrosis factor in terminally differentiating a mouse myeloid leukemic cell line (M1). Evidence that interferon-beta is an autocrine differentiating factor.  J Immunol. 1988;  140 112-119
  • 22 Peters C, Lotzerich H, Niemeier B, Schule K, Uhlenbruck G. Exercise, cancer and the immune response of monocyte.  Anticancer Res. 1995;  15 175-179
  • 23 Pollock M L, Wilmore J H, Fox S M. Exercise in Health and Disease.  Evaluation and prescription for prevention and rehabilitation. Philadelphia; W. B. Saunders Co. Press 1984: 53-87
  • 24 Saltin B. Physiological effects of physical conditioning.  Med Sci Sports Exerc. 1969;  1 50-56
  • 25 Taetle R, Caviles A, Koziol J. Response of human myeloid leukemia cells to various sources of colony-stimulating activity and phytohemagglutinin-conditioned medium.  Cancer Res. 1983;  43 2350-2357
  • 26 Tvede N, Pedersen B K, Hansen F R . et al . Effect of physical exercise on blood mononuclear cell subpopulation and in vitro proliferative responses.  Scand J Immunol. 1989;  29 383-389
  • 27 Viti A, Muscettola M, Paulesu L, Bocci V, Almi A. Effects of exercise on plasma interferon levels.  J Appl Physiol. 1985;  59 426-428
  • 28 Wang S Y, Chen L Y, Wang S J, Lin C K, Ho C K. Growth inhibition and differentiation in HL-60 leukemia cells induced by 1,25-dihydroxyvitamin D3 and tumor necrosis factor alpha.  Exp Hematol. 1991;  19 122-127
  • 29 Woods J A, Davis J M, Mayer E P, Graffar A, Pate R R. Effects of exercise on macrophage activation for anti-tumor cytotoxicity.  J Appl Physiol. 1994;  76 2177-2185
  • 30 Woods J A, Davis J M. Exercise, monocyte/macrophage function, and cancer.  Med Sci Sports Exerc. 1994;  26 147-157

M.D. Yu-Jen Chen

Department of Radiation Oncology Mackay Memorial Hospital

92 Chung San Road Taipei Taiwan 10449 Republic of China

Fax: Fax:+ 886 (2) 28096180

Email: E-mail:oncoman@ms1.mmh.org.tw

    >