Matamoros N, Milà J, Llano M, Balas A, Vicario J L, Pons J, Crespí C, Martinez N, Iglesias-Alzueta J, López-Botet M
Servicio de Inmunología, Hospital Universitario Son Dureta, Andrea Doria, Palma de Mallorca, Spain.
Clin Exp Immunol. 2001 Aug;125(2):274-82. doi: 10.1046/j.1365-2249.2001.01595.x.
In this paper we describe the clinical and molecular features of a new case (GOR) of homozygous human TAP2 deficiency, analysing the phenotype and function of NK cells. The patient presented from infancy with recurrent sinopulmonary infections; a selective IgG2 deficiency, negative antibody response to polysaccharide vaccination and low level of cell surface expression of HLA class I antigens were found. The sequence of TAP2 gene identified a single mutation, a C to T substitution changing the CGA arg codon at amino acid 220 into TGA stop codon in exon 3. By using MoAbs for KIRs, CD94, CD94/NKG2A and ILT2 we observed, in agreement with others, that the latter two receptors were overexpressed on TAP2-deficient NK cells. The inhibitory CD94/NKG2A and triggering CD94/NKG2C NK receptors, specific for HLA-E, appeared to be functional in a limited number of NK clones that could be expanded in vitro. Expression of HLA-E was virtually undetectable in GOR B-LCL and very faint in PBMC, further supporting that interactions of class I leader sequence nonamers with HLA-E in the ER depend on a functional TAP complex.
在本文中,我们描述了一例纯合型人类TAP2缺陷新病例(GOR)的临床和分子特征,分析了自然杀伤细胞(NK细胞)的表型和功能。该患者自婴儿期起就反复出现鼻窦肺部感染;发现存在选择性IgG2缺陷、对多糖疫苗接种的抗体反应阴性以及HLA I类抗原的细胞表面表达水平较低。TAP2基因序列鉴定出一个单一突变,即外显子3中第220位氨基酸处的CGA精氨酸密码子突变为TGA终止密码子,由C到T的替换。通过使用针对杀伤细胞免疫球蛋白样受体(KIRs)、CD94、CD94/NKG2A和免疫球蛋白样转录体2(ILT2)的单克隆抗体(MoAbs),我们与其他人的观察结果一致,发现后两种受体在TAP2缺陷的NK细胞上过度表达。对HLA-E具有特异性的抑制性CD94/NKG2A和激活性CD94/NKG2C NK受体,在少数可在体外扩增的NK克隆中似乎具有功能。在GOR B淋巴母细胞系(B-LCL)中几乎检测不到HLA-E的表达,在外周血单个核细胞(PBMC)中表达非常微弱,这进一步支持了内质网(ER)中I类前导序列九聚体与HLA-E的相互作用依赖于功能性TAP复合物。