BACKGROUND AND OBJECTIVE: Over the past few years, the importance of
interleukin-22 (IL-22) and T-helper (Th)22 lymphocytes in the pathogenesis of
periodontitis has become apparent; however, there are still aspects that are not
addressed yet. Cells expressing IL-22 and aryl hydrocarbon receptor (AhR),
transcription factor master switch gene implicated in the differentiation and
function of Th22 lymphocytes, have been detected in periodontal tissues of
periodontitis-affected patients. In addition, IL-22 has been associated with
osteoclast differentiation and their bone resorptive activity in vitro. However,
the destructive potential of IL-22-expressing AhR+ Th22 lymphocytes over
periodontal tissues during periodontitis has not been demonstrated in vivo yet.
Therefore, this study aimed to analyze whether IL-22-expressing CD4+ AhR+ T
lymphocytes detected in periodontal lesions are associated with alveolar bone
resorption during experimental periodontitis.
MATERIAL AND METHODS: Using a murine model of periodontitis, the expression
levels of IL-22 and AhR, as well as the Th1-, Th2-, Th17- and T
regulatory-associated cytokines, were analyzed in periodontal lesions using
qPCR. The detection of CD4+ IL-22+ AhR+ T lymphocytes was analyzed in
periodontal lesions and cervical lymph nodes that drain these periodontal
lesions using flow cytometry. In addition, the expression of the
osteoclastogenic mediator called receptor activator of nuclear factor-κB ligand
(RANKL) was analyzed by qPCR, western blot, and immunohistochemistry. Finally,
alveolar bone resorption was analyzed using micro-computed tomography and
scanning electron microscopy, and the bone resorption levels were correlated
with IL-22 and RANKL expression.
RESULTS: Higher levels of IL-22, AhR, and RANKL, as well as IL-1β, IL-6, IL-12,
IL-17, IL-23, and TNF-α, were expressed in periodontal lesions of infected mice
compared with periodontal tissues of sham-infected and non-infected controls.
Similarly, high RANKL immunoreaction was observed in periodontal tissues of
infected mice; however, few or absent RANKL immunoreaction was observed in
controls. This association between RANKL and periodontal infection was ratified
by western blot. Furthermore, a higher detection of CD4+ IL-22+ AhR+ T
lymphocytes was found in periodontal lesions and cervical lymph nodes that drain
these periodontal lesions in infected mice compared with non-infected controls.
Finally, the increased IL-22 and RANKL expression showed positive correlation
between them and with the augmented alveolar bone resorption observed in
experimental periodontal lesions.
CONCLUSION: This study demonstrates the increase of IL-22-expressing CD4+ AhR+ T
lymphocytes in periodontitis-affected tissues and shows a positive correlation
between IL-22, RANKL expression, and alveolar bone resorption.