Henry Charles H, Nikaein Afzal, Wolford Larry M
Baylor University Medical Center Transplantation Laboratory, Dallas, TX, USA.
J Oral Maxillofac Surg. 2002 Jul;60(7):778-83. doi: 10.1053/joms.2002.33245.
Spondyloarthropathy includes the subcategory of reactive arthritis (ReA). Spondyloarthropathies are commonly associated with certain human leukocyte antigen (HLA) alleles. Because we identified bacteria associated with ReA within the temporomandibular joint (TMJ), we now evaluate the frequency of HLA alleles in patients with TMJ pathology.
HLA typing of 129 patients (121 females and 8 males) performed by standard microcytotoxicity technique. Thirty patients had only class I (HLA-A and -B loci) evaluated. Ninety-nine patients had both class I and class II (HLA-DR loci) evaluated. Identification of alleles at the C locus was not performed. The antigenic frequency in the study group was compared to US white control subjects using a 2-tailed Fisher's exact test with a Bonferroni multiple comparison adjustment.
The following class I HLA alleles, -A1 (32%), -A2 (50%), -A3 (33%), -B7 (23%), -B14 (14%), -B35 (20%), and -B44 (36%), including the B7 cross-reactive group (CREG) (49%) and class II alleles -DR1 (25%) and -DR4 (34%), were found to have an increased frequency in our patient group.
Our study shows an increased frequency of several alleles that have been previously associated with arthropathy, and the alleles of the B7 CREG, in patients with TMJ pathology. Patients with these alleles may have an increased risk for the development of internal derangement of the TMJ as a consequence of the bacterial/infectious agents and host interactions with the subsequent cytokine/inflammatory response being influenced by their HLA phenotype.
脊柱关节病包括反应性关节炎(ReA)这一亚类。脊柱关节病通常与某些人类白细胞抗原(HLA)等位基因相关。由于我们在颞下颌关节(TMJ)中发现了与ReA相关的细菌,我们现在评估TMJ病理患者中HLA等位基因的频率。
采用标准微细胞毒性技术对129例患者(121例女性和8例男性)进行HLA分型。30例患者仅评估了I类(HLA - A和 - B位点)。99例患者同时评估了I类和II类(HLA - DR位点)。未进行C位点等位基因的鉴定。使用双尾Fisher精确检验并进行Bonferroni多重比较调整,将研究组中的抗原频率与美国白人对照受试者进行比较。
在我们的患者组中发现以下I类HLA等位基因频率增加: - A1(32%)、 - A2(50%)、 - A3(33%)、 - B7(23%)、 - B14(14%)、 - B35(20%)和 - B44(36%),包括B7交叉反应组(CREG)(49%)以及II类等位基因 - DR1(25%)和 - DR4(34%)。
我们的研究表明,在TMJ病理患者中,几种先前与关节病相关的等位基因以及B7 CREG的等位基因频率增加。具有这些等位基因的患者由于细菌/感染因子以及宿主相互作用,随后细胞因子/炎症反应受其HLA表型影响,可能发生TMJ内紊乱的风险增加。