Waltimo Elin, Eray Mine, Mäkitie Antti, Haglund Caj, Atula Timo, Hagström Jaana
Department of Oral and Maxillofacial Diseases, University of Helsinki, Helsinki, Finland.
Department of Pathology, University of Helsinki and Helsinki University Hospital, Helsinki, Finland.
J Oral Microbiol. 2024 Jul 24;16(1):2382633. doi: 10.1080/20002297.2024.2382633. eCollection 2024.
The association of chronic sclerosing sialadenitis and IgG4-related disease (IgG4-RD) has resulted in the more frequent identification of IgG4-positivity in submandibular gland inflammations, also uncovering IgG4 overexpression in nonspecific inflammations. These findings lead us to hypothesise that IgG4-positive sialadenitis represents a continuous inflammatory process overlapping histologically with IgG4-RD, possibly differing in aetiology. However, the antigen underlying IgG4 overexpression in IgG4-positive sialadenitis and IgG4-RD remains unknown.
Here, we investigated toll-like receptor (TLR) - mediated bacterial inflammation in submandibular gland tissues of patients with IgG4-positive and IgG4-negative chronic inflammatory lesions of the submandibular gland ( = 61), with noninflamed submandibular glands serving as controls ( = 4). Utilising immunohistochemistry, we assessed the expression of TLR2 and TLR4, lipopolysaccharide (LPS) and the -specific antigen gingipain R1.
We observed TLR2- and TLR4-immunopositivity in 64 (98%) samples. However, TLR2 and TLR4 staining intensity was significantly stronger in the IgG4-positive group. LPS- and gingipain R1 immunopositivity were observed in 56 (86%) and 58 (89%) samples, respectively. LPS-positivity localised exclusively in mast cell-like cells, while gingipain R1-positivity remained scarce.
A stronger TLR2 or TLR4 expression in IgG4-positive sialadenitis may indicate a tissue-related factor underlying this form of chronic sialadenitis. LPS- and immunopositivity remained weak throughout this series. Thus, gram-negative bacteria may not represent pathogens underlying these forms of chronic sialadenitis.
慢性硬化性涎腺炎与IgG4相关疾病(IgG4-RD)的关联使得在颌下腺炎症中更频繁地发现IgG4阳性,同时也揭示了非特异性炎症中IgG4的过度表达。这些发现使我们推测IgG4阳性涎腺炎代表一种与IgG4-RD在组织学上重叠的连续炎症过程,病因可能不同。然而,IgG4阳性涎腺炎和IgG4-RD中IgG4过度表达的抗原仍不清楚。
在此,我们研究了 Toll样受体(TLR)介导的细菌炎症在颌下腺IgG4阳性和IgG4阴性慢性炎症病变患者(n = 61)的颌下腺组织中的情况,以未发炎的颌下腺作为对照(n = 4)。利用免疫组织化学,我们评估了TLR2和TLR4、脂多糖(LPS)以及特异性抗原牙龈蛋白酶R1的表达。
我们在64个(98%)样本中观察到TLR2和TLR4免疫阳性。然而,TLR2和TLR4染色强度在IgG4阳性组中显著更强。分别在56个(86%)和58个(89%)样本中观察到LPS和牙龈蛋白酶R1免疫阳性。LPS阳性仅定位于肥大细胞样细胞,而牙龈蛋白酶R1阳性仍然很少见。
IgG4阳性涎腺炎中TLR2或TLR4表达更强可能表明这种慢性涎腺炎形式存在组织相关因素。在整个系列中LPS和免疫阳性仍然较弱。因此,革兰氏阴性菌可能不是这些慢性涎腺炎形式的病原体。