Rj. Koch et L. Brodsky, QUALITATIVE AND QUANTITATIVE IMMUNOGLOBULIN PRODUCTION BY SPECIFIC BACTERIA IN CHRONIC TONSILLAR DISEASE, The Laryngoscope, 105(1), 1995, pp. 42-48
Tonsillar tissue lymphocyte (TTL) function as measured by immunoglobul
in production was assessed in vitro in 60 tonsils, 51 diseased and 9 n
ormal controls. The diseased specimens were from children (aged 3 to 1
0 years) clinically classified as having recurrent tonsillitis (RT), i
diopathic tonsillar hyperplasia (ITH), or recurrent tonsillitis with h
yperplasia (RT/H). TTLs were challenged with intact, heat-inactivated
bacteria found in the core of diseased tonsils-Streptococcus pyogenes
(SP) and Haemophilus influenzae type B (HIB) as well as the dominant b
acterium (DB) grown from that particular tonsillar core. The phytomito
gen, leukoagglutinin (LA), was used as a nonspecific activator. Qualit
ative immunoglobulin production was assessed for the immunoglobulin G
(IgG), immunoglobulin M (IgM), and immunoglobulin A (IgA) classes. Imm
unoglobulin-specific production was quantified at the basal level, and
at 2, 4, and 6 days following stimulation. Stimulation with HIB produ
ced the greatest amount of IgG and IgM in TTLs from control tonsils. T
he DB was a relatively weak stimulator of normal (control) TTLs, yet p
roduced relatively brisk IgG responses in the RT and ITH categories. I
t did, however, yield only marginal IgM secretion in these groups. IgA
was consistently produced after stimulation in diseased TTLs, yet was
not elicited from normal TTLs. The aforementioned findings suggest a
differential qualitative and quantitative immunoglobulin response for
healthy, recurrently infected, and hyperplastic tonsils. Lymphocyte hy
pofunction along with structural changes associated with hyperplasia m
ay be central to the etiology of chronic tonsillar disease. The tonsil
lar immunologic response in disease and health is discussed.