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Effects of serum from HIV-infected subjects on the functional activity of polymorphonuclear neutrophils

E C Pieri1, M A Orsilles

  • 1Laboratorio de Inmunologia, Hospital Rawson, Córdoba, Argentina.

Journal of Clinical & Laboratory Immunology
|January 1, 1995
PubMed

Insights

Polymorphonuclear neutrophils (PMN) from HIV-seropositive patients show normal function. However, serum factors in asymptomatic infection and AIDS patients can alter PMN activity, impacting immune response.

Area of Science:

  • Immunology
  • Infectious Diseases
  • Cell Biology

Background:

  • Polymorphonuclear neutrophils (PMN) are crucial for innate immunity.
  • Assessing PMN oxidative capacity is vital for understanding immune function in HIV infection.
  • Previous studies suggest potential PMN dysfunction in acquired immunodeficiency syndrome (AIDS).

Purpose of the Study:

  • To evaluate the oxidative capacity of PMN in individuals with asymptomatic HIV infection (AI) and AIDS.
  • To investigate the influence of patient serum on the functional activity of normal and patient PMN.
  • To determine if PMN dysfunction is intrinsic or serum-mediated in HIV-seropositive individuals.

Main Methods:

  • Quantitative Nitroblue Tetrazolium (NBT) reduction test was employed.
  • PMN oxidative capacity was assessed in unstimulated and zymosan-stimulated conditions.
  • The effect of serum from AI and AIDS patients on normal and patient PMN was analyzed.

Main Results:

  • PMN oxidative capacity was comparable between AI, AIDS patients, and healthy controls when using normal serum.
  • Serum from 65% of AI subjects increased stimulated NBT reduction in PMN.
  • Serum from 50% of AIDS patients decreased stimulated NBT reduction in PMN.
  • These serum effects were not correlated with complement C3 or immune complex levels.

Conclusions:

  • PMN from HIV-seropositive patients do not exhibit intrinsic functional defects.
  • Serum factors in AI and AIDS patients can modulate PMN functional activity.
  • The stage of HIV infection influences serum-mediated effects on PMN function.

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