Suleiman Al-Hammadi, Najla S Alkuwaiti, Ghassan A Ghatasheh, Huda Al Dhanhani, Hiba M Shendi, Abdulghani S Elomami, Farida Almarzooqi, Abdul-Kader Souid
{"title":"卡介苗和轮状病毒疫苗在先天性免疫错误婴儿中的不良反应","authors":"Suleiman Al-Hammadi, Najla S Alkuwaiti, Ghassan A Ghatasheh, Huda Al Dhanhani, Hiba M Shendi, Abdulghani S Elomami, Farida Almarzooqi, Abdul-Kader Souid","doi":"10.1155/2020/8857152","DOIUrl":null,"url":null,"abstract":"<p><strong>Background: </strong>The Bacillus Calmette-Guérin (BCG) and rotavirus vaccines are live-attenuated preparations. In the United Arab Emirates, these products are universally administered to the young infants. This unguided practice does not account for the children with immunodeficiency, which frequently manifests after the administration of these vaccines. We present here a young infant with immunodeficiency that developed disseminated tuberculosis infection and severe diarrhea due to these improper immunizations. <i>Case Presentation</i>. This young infant was diagnosed at six months of age with \"immunodeficiency type 19\" (MIM#615617) due to homozygous nonsense variant, NM_000732.4 (<i>CD3D</i>):c.128G > A, p.Trp43∗ (variation ClinVar#VCV000643120.1; pathogenic). This variant creates premature stop-gain in <i>CD3D</i> (CD3 antigen, delta subunit, autosomal recessive; MIM#186790), resulting in loss-of-function. He also had \"<i>X</i>-linked agammaglobulinemia\" (MIM#300755) due to hemizygous missense variant, NM_001287344.1 (<i>BTK</i>):c.80G > A, p.Gly27Asp (novel). He had a sibling who passed away in infancy of unknown disease and family members with autoimmune disorders. Despite these clear clues, he was immunized with BCG at birth and rotavirus at 2 and 4 months. He was well in the first four months. He then developed high-fever, lymphadenopathy, and refractory diarrhea. Stool was positive for rotavirus, and lymph node biopsy showed acid-fast bacilli, consistent with tuberculosis lymphadenitis. These infections were serious and markedly complicated his clinical course, which included bone marrow transplantation from a matched sibling.</p><p><strong>Conclusions: </strong>These unfortunate events could have been avoided by compiling the available clinical information. This patient underscores the importance of implementing proper policies for BCG and rotavirus vaccinations. International registries of adverse events of universally administered vaccines are crucial.</p>","PeriodicalId":0,"journal":{"name":"","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"2020-11-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1155/2020/8857152","citationCount":"4","resultStr":"{\"title\":\"Adverse Events of the BCG (Bacillus Calmette-Guérin) and Rotavirus Vaccines in a Young Infant with Inborn Error of Immunity.\",\"authors\":\"Suleiman Al-Hammadi, Najla S Alkuwaiti, Ghassan A Ghatasheh, Huda Al Dhanhani, Hiba M Shendi, Abdulghani S Elomami, Farida Almarzooqi, Abdul-Kader Souid\",\"doi\":\"10.1155/2020/8857152\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><strong>Background: </strong>The Bacillus Calmette-Guérin (BCG) and rotavirus vaccines are live-attenuated preparations. In the United Arab Emirates, these products are universally administered to the young infants. This unguided practice does not account for the children with immunodeficiency, which frequently manifests after the administration of these vaccines. We present here a young infant with immunodeficiency that developed disseminated tuberculosis infection and severe diarrhea due to these improper immunizations. <i>Case Presentation</i>. This young infant was diagnosed at six months of age with \\\"immunodeficiency type 19\\\" (MIM#615617) due to homozygous nonsense variant, NM_000732.4 (<i>CD3D</i>):c.128G > A, p.Trp43∗ (variation ClinVar#VCV000643120.1; pathogenic). This variant creates premature stop-gain in <i>CD3D</i> (CD3 antigen, delta subunit, autosomal recessive; MIM#186790), resulting in loss-of-function. He also had \\\"<i>X</i>-linked agammaglobulinemia\\\" (MIM#300755) due to hemizygous missense variant, NM_001287344.1 (<i>BTK</i>):c.80G > A, p.Gly27Asp (novel). He had a sibling who passed away in infancy of unknown disease and family members with autoimmune disorders. Despite these clear clues, he was immunized with BCG at birth and rotavirus at 2 and 4 months. He was well in the first four months. He then developed high-fever, lymphadenopathy, and refractory diarrhea. Stool was positive for rotavirus, and lymph node biopsy showed acid-fast bacilli, consistent with tuberculosis lymphadenitis. These infections were serious and markedly complicated his clinical course, which included bone marrow transplantation from a matched sibling.</p><p><strong>Conclusions: </strong>These unfortunate events could have been avoided by compiling the available clinical information. This patient underscores the importance of implementing proper policies for BCG and rotavirus vaccinations. International registries of adverse events of universally administered vaccines are crucial.</p>\",\"PeriodicalId\":0,\"journal\":{\"name\":\"\",\"volume\":null,\"pages\":null},\"PeriodicalIF\":0.0,\"publicationDate\":\"2020-11-28\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://sci-hub-pdf.com/10.1155/2020/8857152\",\"citationCount\":\"4\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.1155/2020/8857152\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"2020/1/1 0:00:00\",\"PubModel\":\"eCollection\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1155/2020/8857152","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2020/1/1 0:00:00","PubModel":"eCollection","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 4
摘要
背景:卡介苗和轮状病毒疫苗均为减毒活疫苗。在阿拉伯联合酋长国,这些产品普遍适用于年幼的婴儿。这种无指导的做法没有考虑到免疫缺陷儿童,免疫缺陷儿童经常在接种这些疫苗后出现。我们在此报告一个年轻的婴儿免疫缺陷,发展播散性结核感染和严重腹泻,由于这些不当的免疫接种。案例演示。这名婴儿在6个月大时被诊断为“免疫缺陷19型”(MIM#615617),原因是纯合无义变异NM_000732.4 (CD3D):c。128G > A, p.Trp43 *(变异ClinVar#VCV000643120.1;致病性)。该变异在CD3D (CD3抗原,δ亚基,常染色体隐性)中产生过早停止增益;MIM#186790),导致功能丧失。由于半合子错义变异,NM_001287344.1 (BTK):c,他还患有“x连锁无球蛋白血症”(MIM#300755)。80G > A, p.Gly27Asp(新)。他有一个兄弟姐妹在婴儿期因未知疾病去世,家庭成员也患有自身免疫性疾病。尽管有这些明确的线索,他还是在出生时接种了卡介苗,在2个月和4个月时接种了轮状病毒。头四个月他身体很好。随后出现高热、淋巴结病和难治性腹泻。粪便轮状病毒阳性,淋巴结活检显示抗酸杆菌,符合结核性淋巴结炎。这些感染很严重,明显地使他的临床过程复杂化,其中包括从一个匹配的兄弟姐妹那里移植骨髓。结论:这些不幸的事件是可以通过整理现有的临床资料来避免的。该患者强调了实施适当的卡介苗和轮状病毒疫苗接种政策的重要性。对普遍接种疫苗的不良事件进行国际登记至关重要。
Adverse Events of the BCG (Bacillus Calmette-Guérin) and Rotavirus Vaccines in a Young Infant with Inborn Error of Immunity.
Background: The Bacillus Calmette-Guérin (BCG) and rotavirus vaccines are live-attenuated preparations. In the United Arab Emirates, these products are universally administered to the young infants. This unguided practice does not account for the children with immunodeficiency, which frequently manifests after the administration of these vaccines. We present here a young infant with immunodeficiency that developed disseminated tuberculosis infection and severe diarrhea due to these improper immunizations. Case Presentation. This young infant was diagnosed at six months of age with "immunodeficiency type 19" (MIM#615617) due to homozygous nonsense variant, NM_000732.4 (CD3D):c.128G > A, p.Trp43∗ (variation ClinVar#VCV000643120.1; pathogenic). This variant creates premature stop-gain in CD3D (CD3 antigen, delta subunit, autosomal recessive; MIM#186790), resulting in loss-of-function. He also had "X-linked agammaglobulinemia" (MIM#300755) due to hemizygous missense variant, NM_001287344.1 (BTK):c.80G > A, p.Gly27Asp (novel). He had a sibling who passed away in infancy of unknown disease and family members with autoimmune disorders. Despite these clear clues, he was immunized with BCG at birth and rotavirus at 2 and 4 months. He was well in the first four months. He then developed high-fever, lymphadenopathy, and refractory diarrhea. Stool was positive for rotavirus, and lymph node biopsy showed acid-fast bacilli, consistent with tuberculosis lymphadenitis. These infections were serious and markedly complicated his clinical course, which included bone marrow transplantation from a matched sibling.
Conclusions: These unfortunate events could have been avoided by compiling the available clinical information. This patient underscores the importance of implementing proper policies for BCG and rotavirus vaccinations. International registries of adverse events of universally administered vaccines are crucial.