Background: Interleukin 16 (IL-16) acts highly chemotactic on CD4-bearing c
ells. Besides chemotaxis, IL-16 has numerous immunomodulatory effects, and
not only on T cells.
Objective: To determine IL-16 expression in human tonsils.
Methods: Tonsillar follicles were immunohistologically characterized to eli
cit a possible cellular source of IL-16 expression.
Results: The mantle zone of immature and mature B cells was CD22 immunoreac
tive (ir), whereas the germinal center of activated B cells was CD23-ir. Pl
asma cells that were CD38-ir were observed extrafollicularly beneath the ep
ithelium and within the germinal center. T cells were found most frequently
in the extrafollicular space, with a majority of CD4 cells. CD68-ir macrop
hages were predominantly found within the germinal center. Immunostaining o
f anti-IL-16 revealed strong cytoplasmatic reactivity of extrafollicular ce
lls and of cells at the outer rim of the mantle zone. Numerous cells adhere
nt to the stratified squamous epithelium were IL-16-ir as well. Double immu
nostaining identified CD4(+) T cells as the major cellular source of IL-16
expression. Furthermore, a population of CD22(+) B cells at the outer rim o
f the mantle zone expressed IL-16 as well.
Conclusions: Interleukin 16 was mainly expressed in a typical CD4-like patt
ern in human tonsils. Our data strongly suggest that CD4(+) lymphocytes con
stitute the major cellular source for IL-16. We hypothesize that the double
-immunostained CD4-ir and IL-16-ir cells represent activated T cells. Becau
se CD22(+) B cells at the outer rim of the mantle zone expressed IL-16 as w
ell, we conclude that this area might constitute the locus of IL-16-mediate
d B-cell differentiation.