HUMORAL IMMUNITY TO COMMENSAL ORAL BACTERIA IN HUMAN INFANTS - SALIVARY ANTIBODIES REACTIVE WITH ACTINOMYCES-NAESLUNDII GENOSPECIES-1 AND GENOSPECIES-2 DURING COLONIZATION
Mf. Cole et al., HUMORAL IMMUNITY TO COMMENSAL ORAL BACTERIA IN HUMAN INFANTS - SALIVARY ANTIBODIES REACTIVE WITH ACTINOMYCES-NAESLUNDII GENOSPECIES-1 AND GENOSPECIES-2 DURING COLONIZATION, Infection and immunity, 66(9), 1998, pp. 4283-4289
The secretory immune response in saliva to colonization by Actinomyces
naeslundii genospecies 1 and 2 was studied in 10 human infants from b
irth to 2 years of age. Actinomyces species were not recovered from th
e mouths of the infants until approximately 4 months after the eruptio
n of teeth. However, low levels of secretory immunoglobulin Al (SIgA1)
and SIgA2 antibodies reactive with whole cells of A. naeslundii genos
pecies 1 and 2 were detected within the first month after birth, Altho
ugh there was a fivefold increase in the concentration of SIgA between
birth and age 2 years, there were no differences between the concentr
ations of SIgA1 and SIgA2 antibodies reactive with A. naeslundii genos
pecies 1 and 2 over this period, When the concentrations of SIgA1 and
SIgA2 antibodies reactive with whole cells of A. naeslundii genospecie
s 1 and 2 were normalized to the concentrations of SIgA1 and SIgA2 in
saliva, the A. naeslundii genospecies 1- and 2-reactive SIgA1 and SIgA
2 antibodies showed a significant decrease from birth to 2 years of ag
e. The fine specificities of A, naeslundii genospecies 1- and 2-reacti
ve SIgA1 and SIgA2 antibodies were examined by Western blotting of env
elope proteins. Similarities in the molecular masses of proteins recog
nized by SIgA1 and SIgA2 antibodies, both within and between subjects
over time, were examined by cluster analysis and showed considerable v
ariability. Taken overall, our data suggest that among the mechanisms
Actinomyces species employ to persist in the oral cavity are the induc
tion of a limited immune response and clonal replacement with strains
differing in their antigen profiles.