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Natural killer cells after ALTAIR mission
I V Konstantinova1, M Rykova, D Meshkov
1IBMP, Moscow, Russia.
Acta Astronautica
|October 1, 1995
Summary
Space flight impacts natural killer (NK) cell activity, reducing their cytotoxic function and cell counts. This immune system alteration may be linked to defective NK cell function or fewer circulating effector cells post-flight.
Area of Science:
- Immunology
- Space Medicine
- Cellular Biology
Background:
- Reduced in vitro natural killer (NK) cytotoxic activity is a known consequence of both prolonged and short-term space flights.
- Understanding the specific effects of space travel on immune cell function is crucial for astronaut health.
Purpose of the Study:
- To investigate the impact of space flight on NK cell functions, counts, and the production of Interleukin-2 (IL-2) and Tumor Necrosis Factor (TNF) by lymphocytes.
- To assess immune responses in French and Russian cosmonauts after varying durations of space missions.
Main Methods:
- Analysis of NK cell cytotoxic activity, target cell binding and lysis capacity, and NK cell percentages.
- Measurement of IL-2 and TNF production by lymphocytes stimulated with specific agents (PMA, PHA).
- Immunological examinations of cosmonauts before and after space flight.
Main Results:
- A French cosmonaut showed decreased NK cell cytotoxic activity, target cell interaction, and NK cell percentage after a 21-day flight.
- This cosmonaut also exhibited a twofold reduction in TNF production stimulated by PMA and PHA/PMA, but not in 48-hour PHA-stimulated cultures.
- IL-2 biological activity remained unchanged, and no significant deviations were found in two Russian cosmonauts after a 197-day flight.
Conclusions:
- Space flight can lead to reduced NK cell cytotoxic activity and potentially fewer circulating effector cells.
- While some immune functions like TNF and IL-2 production may be resilient, others are demonstrably affected by space exposure.
- Further research is needed to fully elucidate the mechanisms behind space flight-induced immune alterations.