L. Hsiung et al., FLOW CYTOMETRIC ANALYSIS OF LYMPHOCYTE SUBSETS OF MICE MAINTAINED ON AN ETHANOL-CONTAINING LIQUID DIET, Alcoholism, clinical and experimental research, 18(1), 1994, pp. 12-20
Alcoholic patients often have impaired immune function, yet little is
known about the precise mechanism(s) of this impairment. We have previ
ously shown that ethanol consumption by mice alters copolymer-specific
humoral and cellular immune responses. In this study, we asked whethe
r alcohol consumption by mice would phenotypically alter lymphocyte po
pulations. Female C57BL/6 mice were fed a nutritionally complete liqui
d diet containing 35% ethanol-derived calories for up to 8 days. As co
ntrols, mice either were fed a liquid control diet that isocalorically
substitutes sucrose for ethanol or remained on a standard solid diet
end water ad libitum. Although mice fed ethanol-containing liquid or p
air-fed control liquid diets have decreased numbers of spleen cells co
mpared with solid diet controls, only the ethanol-containing diet allo
wed normally nonresponder C57BL/6 spleen cells to make antibody respon
ses to the poly(Glu(50)Tyr(50)) synthetic copolymer antigen. Flow cyto
metric analysis of splenic lymphocyte populations of mice on the ethan
ol-containing diet shows an increase in the relative proportion of T-l
ymphocytes as compared with mice on either solid or liquid control die
ts. No such change is seen for either B cell or natural killer cell po
pulations in these same mice. Both liquid control and liquid ethanol d
iets caused a slight decrease in the CD4:CD8 ratios of splenic T-lymph
ocytes. We see the relative percentage of T-cells bearing the alpha be
ta T-cell receptor (TcR) increases in the spleens of liquid ethanol di
et mice; a smaller increase TcR alpha beta usage is seen in the spleen
s of liquid control mice, compared with solid diet mice. Flow cytometr
ic analysis shows that little, if any, difference exists in TcR gamma
delta expression between the liquid ethanol and either the liquid cont
rol or solid diet groups. Preliminary analysis of TcR alpha beta subse
ts suggest that ethanol increases the percentage of T-cells expressing
V beta 5 and V beta 8, and decreases the percentage of V beta 11 expr
essing cells. These findings suggest that, in addition to modifying th
e immune response, ethanol alters the phenotypic expression of lymphoc
yte subsets.