B. Woodward et al., T cells with a quiescent phenotype (CD45RA(+)) are overabundant in the blood and involuted lymphoid tissues in wasting protein and energy deficiencies, IMMUNOLOGY, 96(2), 1999, pp. 246-253
The objective of this investigation was to determine the influence of disti
nct forms of acute weight loss on the expression of the quiescence marker,
CD45RA, by T cells in several lymphoid compartments including the blood. Ma
le and female weanling mice, CBA/J and C57BL/6J strains, were allocated to
the following groups: acl libitum intake of a complete purified diet: restr
icted intake of the complete diet; and ad libitum intake of an isocaloric l
ow-protein diet. The restricted intake protocol produced weight loss throug
h energy deficiency (marasmic-type malnutrition), whereas the low-protein d
iet caused wasting through inadequate protein nitrogen and induced a condit
ion mimicking incipient kwashiorkor. In one experiment, weanling mice of bo
th strains were maintained for 14 days according to each of these dietary p
rotocols and, in a supplementary study, C57BL/6J weanlings consumed either
the complete diet or the low-protein diet Lrtl lihiirllil for 21 days. Zero
-time control groups (19-days old and 23-days old in C57BL/6J and CBA/J str
ains, respectively) were included in the first experiment to control for on
togeny-related change. Expression of CD45RA was assessed by two-colour flow
cytometry in CD4(+) and CD8(+) T cells from the spleen, mesenteric lymph n
odes and blood. Within 14 days, energy-restricted mice exhibited a high per
centage of CD4(+) T cells expressing CD45RA in all three lymphoid compartme
nts in both mouse strains (an average of 50% CD45RA(+) versus 9% in well-no
urished controls), and a similar outcome was apparent in the CD8(+) subset
(93%;, CD45RA(+) versus 63%). Mice fed the low-protein diet required up to
21 days to exhibit the same imbalance within the CD4(+) T-cell subset (33%
CD45RA(+) versus 4% in well-nourished controls). A shift toward a quiescent
phenotype occurs throughout the peripheral T-cell system in acute wasting
disease. Consequently, the quiescence-activation phenotype of blood T cells
reflects the same index in secondary lymphoid organs in such pathologies.
Naive-type quiescence among T cells is implicated as a component of depress
ed adaptive immunocompetence in the advanced stages of diverse forms of acu
te weight loss.