Blanco C, Diaz-Perales A, Collada C, Sánchez-Monge R, Aragoncillo C, Castillo R, Ortega N, Alvarez M, Carrillo T, Salcedo G
Sección de Alergia, Unidad de Investigación, Hospital Nuestra Señora del Pino, Las Palmas de Gran Canaria, Spain.
J Allergy Clin Immunol. 1999 Mar;103(3 Pt 1):507-13. doi: 10.1016/s0091-6749(99)70478-1.
Latex-fruit cross-sensitization has been fully demonstrated. However, the antigens responsible for this "latex-fruit syndrome" have not been identified. We have recently shown that class I chitinases are relevant chestnut and avocado allergens.
We sought to evaluate the in vivo and in vitro reactions of purified chestnut and avocado chitinases in relation to the latex-fruit syndrome.
From a latex-allergic population, eighteen patients allergic to chestnut, avocado, or both were selected. Skin prick tests (SPTs) were performed with crude chestnut and avocado extracts, chitinase-enriched preparations, and purified class I and II chitinases from both fruits. CAP-inhibition assays with the crude extracts and purified proteins were carried out. Immunodetection with sera from patients with latex-fruit allergy and immunoblot inhibition tests with a latex extract were also performed. Eighteen subjects paired with our patients and 15 patients allergic to latex but not food were used as control groups.
The chestnut class I chitinase elicited positive SPT responses in 13 of 18 patients with latex-fruit allergy (72%), and the avocado class I chitinase elicited positive responses in 12 of 18 (67%) similarly allergic patients. By contrast, class II enzymes without a hevein-like domain did not show SPT responses in the same patient group. Each isolated class I chitinase reached inhibition values higher than 85% in CAP inhibition assays against the corresponding food extract in solid phase. Immunodetection of the crude extracts and the purified class I chitinases revealed a single 32-kd band for both chestnut and avocado. Preincubation with a natural latex extract fully inhibited the IgE binding to the crude extracts, as well as to the purified chestnut and avocado class I chitinases.
Chestnut and avocado class I chitinases with an N-terminal hevein-like domain are major allergens that cross-react with latex. Therefore they are probably the panallergens responsible for the latex-fruit syndrome.
乳胶-水果交叉致敏已得到充分证实。然而,导致这种“乳胶-水果综合征”的抗原尚未确定。我们最近发现,I类几丁质酶是相关的栗子和鳄梨过敏原。
我们试图评估纯化的栗子和鳄梨几丁质酶与乳胶-水果综合征相关的体内和体外反应。
从乳胶过敏人群中,选取18名对栗子、鳄梨或两者都过敏的患者。用粗制栗子和鳄梨提取物、富含几丁质酶的制剂以及从这两种水果中纯化的I类和II类几丁质酶进行皮肤点刺试验(SPT)。用粗提取物和纯化蛋白进行CAP抑制试验。还对乳胶-水果过敏患者的血清进行免疫检测,并用乳胶提取物进行免疫印迹抑制试验。18名与我们的患者配对的受试者和15名对乳胶过敏但对食物不过敏的患者作为对照组。
栗子I类几丁质酶在18例乳胶-水果过敏患者中的13例(72%)中引起阳性SPT反应,鳄梨I类几丁质酶在18例类似过敏患者中的12例(67%)中引起阳性反应。相比之下,没有类橡胶素样结构域的II类酶在同一患者组中未显示SPT反应。在针对相应食物提取物的固相CAP抑制试验中,每种分离的I类几丁质酶的抑制值均高于85%。对粗提取物和纯化的I类几丁质酶的免疫检测显示,栗子和鳄梨均有一条单一的32-kd条带。用天然乳胶提取物预孵育可完全抑制IgE与粗提取物以及纯化的栗子和鳄梨I类几丁质酶的结合。
具有N端类橡胶素样结构域的栗子和鳄梨I类几丁质酶是与乳胶发生交叉反应的主要过敏原。因此,它们可能是导致乳胶-水果综合征的泛过敏原。