DUODENAL INTRAEPITHELIAL-GAMMA-DELTA T-CELLS AND SOLUBLE CD8, NEOPTERIN, AND BETA-2-MICROGLOBULIN IN SERUM OF IGA-DEFICIENT SUBJECTS WITH OR WITHOUT IGG SUBCLASS DEFICIENCY
De. Nilssen et al., DUODENAL INTRAEPITHELIAL-GAMMA-DELTA T-CELLS AND SOLUBLE CD8, NEOPTERIN, AND BETA-2-MICROGLOBULIN IN SERUM OF IGA-DEFICIENT SUBJECTS WITH OR WITHOUT IGG SUBCLASS DEFICIENCY, Clinical and experimental immunology, 94(1), 1993, pp. 91-98
Expression of the gamma/delta T cell receptor (TCR) on CD3+ intraepith
elial lymphocytes (IELs) was studied by two-colour immunofluorescence
in duodenal tissue sections from healthy (n = 6) or infection-prone (n
= 7) subjects with selective IgA deficiency (IgAD), and subjects (n =
4) with combined IgAD and IgG subclass deficiency. TCRgamma/delta+ IE
L proportions in selective IgAD subjects (median 6.3%, range 1.0-41%)
and in those with combined deficiency (median 4.5%, range 1.2-33%) wer
e well within the range (0.3-38%) for histologically normal controls (
n=11), but the healthy IgAD subgroup tended to show raised TCRgamma/de
lta+ IEL proportions (median 13-6%) compared with the other two subgro
ups. Also the number of TCRgamma/delta+ IELs per intestinal length uni
t was relatively high (median 13.9/mm) in the healthy IgAD subjects, a
nd significantly raised (P < 0.03) compared with controls (median 3.2/
mm). Paired staining revealed that most TCRgamma/delta+ IELs in both s
elective IgAD (98%) and combined deficiency (99%) were CD8-, and a lar
ge fraction (median 84% and 63%, respectively) expressed the Vdelta1/J
delta1-encoded epitope. The total number of CD3+ IELs (mostly CD8+) wa
s similar to controls. IgAD subjects, and especially the healthy subgr
oup, had significantly increased serum concentrations of soluble CD8 (
P<0.0002), neopterin (P<0.005), and beta2-microglobulin (P < 0.007), w
hich was similar to our previous observations in common variable immun
odeficiency, and probably reflected stimulation of cell-mediated immun
ity. In addition, the increased TCRgamma/delta+ IELs might reflect a c
omponent of compensatory surface protection in the healthy IgAD subgro
up.