S. Walrand et al., Specific and nonspecific immune responses to fasting and refeeding differ in healthy young adult and elderly persons, AM J CLIN N, 74(5), 2001, pp. 670-678
Background: Undernutrition is a main cause of immunodeficiency. Many confou
nding factors limit the interpretation of immune function in hospitalized e
lderly patients.
Objective: We compared the effects of short-term fasting and refeeding on l
ymphocyte subset distribution and neutrophil function in healthy subjects.
Design: Seven young adult ((X) over bar +/- SE age: 24 +/- 2 y) and 8 elder
ly (71 +/- 3 y) subjects were fed standardized diets (1.6 X predicted resti
ng energy expenditure; 16% protein) for 7 d. They then fasted for 36 h and
were refed for 4 h (42 kJ/kg). Lymphocyte subsets were quantified by using
fluorochrome-conjugated monoclonal antibodies. Neutrophil chemotactic migra
tion was evaluated by using a 2-compartment chamber. Neutrophil reactive ox
ygen species production was measured by using a luminol-amplified chemilumi
nescence assay and oxidation of 2'7'-dichlorofluorescein diacetate.
Results: Baseline total and cytotoxic T lymphocyte subpopulations were lowe
r in elderly than in adult subjects (P < 0.01). Nutritional state had a sig
nificant effect (P < 0.05) on total, helper, and cytotoxic T and B lymphocy
te counts in all subjects, and the response of lymphocyte subpopulations to
nutritional fluctuations was significantly affected by age. The chemotacti
c index was lowered by fasting in both groups (P < 0.05 compared with basal
values). After refeeding, neutrophil migration was restored in adult but n
ot elderly subjects. The superoxide anion production rate increased with fa
sting and reverted to prefasting values with refeeding in both groups (P <
0.05). Fasting induced a significant decrease in hydrogen peroxide producti
on in stimulated neutrophils that was reversed by refeeding in adult but no
t elderly subjects.
Conclusion: The lack of response of lymphocyte subpopulation counts and neu
trophil function to nutritional changes may help to explain the proneness o
f elderly persons to infection.