Rj. Koch et L. Brodsky, EFFECT OF SPECIFIC BACTERIA ON LYMPHOCYTE-PROLIFERATION IN DISEASED AND NONDISEASED TONSILS, The Laryngoscope, 103(9), 1993, pp. 1020-1026
Tonsillar tissue lymphocyte (TTL) function as measured by lymphocyte p
roliferation was assessed in vitro in 38 tonsils-30 diseased and 8 nor
mal controls. TTLs from diseased and control tonsils were challenged w
ith intact, heat-inactivated bacteria which may be found in the core o
f diseased tonsils these bacteria were Streptococcus pyogenes and Hemo
philus influenzae type B (HIB), as well as the dominant bacterium (DB)
grown from that particular tonsillar core. The phytomitogen leukoaggl
utinin (LA) was used as a nonspecific activator. Lymphocyte proliferat
ion was quantified and reported using a stimulation index (SI) which w
as based upon viable cell counts at 2, 4, and 6 days following inocula
tion. Overall, the greatest degree of lymphocyte proliferation in dise
ased TTLs (SI = .91) was produced by HIB. However, both SP and HIB pro
duced more lymphocyte proliferation in the nondiseased TTLs than in th
e diseased TTLs (P<.01). H influenzae (non-B) and group A beta-hemolyt
ic streptococci were the pathogens most frequently cultured as the dom
inant bacteria from the core of diseased tonsils; Streptococcus virida
ns was most frequently cultured in nondiseased tonsils. The DB caused
greater TTL proliferation in diseased (SI = .89) versus control (SI =
.63) TTLs (P<.001). These findings suggest a differential proliferativ
e response in vitro for diseased and nondiseased TTLs in response to s
pecific bacteria. The role of possibly pathogenic bacteria and commens
als, as well as the implications for clinical disease, are discussed.