The Involvement of the Intestinal Microflora in the Expansion of CD4⁺ T Cells with a-Naive Phenotype in the Periphery

Abstract

It is well known that immune reactivity declines with age. Recently, we demonstrated that the age-related decrease in IL-2 production by CD4⁺ T cells was accompanied by an increased production of IL-4 and interferon-γ,(IFN-γ). This age-related shift in the profile of lymphokine production was related to phenotypic changes within the CD4⁺ T-cell subset, that is, a decrease in the percentage of CD45RB⁺⁺ CD4⁺ T cells and an increase in the percentage of Pgp-1⁺ CD4⁺ T cells. To study whether these age-related changes were due to previous antigenic exposure, we performed a phenotypic and functional analysis on splenic CD4⁺ T cells isolated from individual, germ-free (GF), specific pathogen-free (SPF), and clean conventional (CC) mice. Interestingly, the total number of splenic CD4⁺ T cells in GF mice was twofold lower as compared to age-matched SPF or CC mice, regardless whether mice were analyzed at young (10 weeks) or at advanced age (13-14 months). Unexpectedly, the phenotypic composition of the CD4⁺ T-cell subset was comparable in the GF, SPF, and CC mice as determined by the expression of CD45RB and Pgp-1, indicating that CD4⁺ T cells with a naive phenotype (CD45RB⁺⁺ Pgp-1 ^–) were not enriched in GF mice. Moreover, at an age of 13–14 months, CD4⁺ T cells from GF mice frequently produced more IL-4 and IFN-γ, than their CC counterparts. These lymphokine data showed, therefore, that a relatively high proportion of CD4 T cells with a memory phenotype can also be defined in GF mice on the basis of their function. The contamination of GF mice with a colonization resistant factor (CRF flora) resulted in twofold higher numbers of splenic CD4⁺ T cells. Surprisingly, not only CD4⁺ T cells with a memory phenotype (CD45RB^–/+ Pgp-1⁺⁺) had expanded, but also CD4⁺ T cells with a naive (CD45RB⁺⁺ Pgp-1^–) phenotype. Our results, therefore, strongly suggest that the expansion of naive CD4⁺ T cells in the periphery is mediated by the intestinal microflora.

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