T cells with a quiescent phenotype (CD45RA(+)) are overabundant in the blood and involuted lymphoid tissues in wasting protein and energy deficiencies

Citation
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
Citations number
31
Categorie Soggetti
Immunology
Journal title
IMMUNOLOGY
ISSN journal
00192805 → ACNP
Volume
96
Issue
2
Year of publication
1999
Pages
246 - 253
Database
ISI
SICI code
0019-2805(199902)96:2<246:TCWAQP>2.0.ZU;2-Z
Abstract
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.