Prethika P A, Shastry Shamee, Mohan Ganesh, Prabhu Ravindra Attur, Nagaraju Shankar Prasad, Rangaswamy Dharshan
Department of Immunohematology and Blood Transfusion, Kasturba Medical College, Manipal Academy of Higher Education, Manipal, Karnataka, India.
Department of Nephrology, Kasturba Medical College, Manipal Academy of Higher Education, Manipal, Karnataka, India.
Asian J Transfus Sci. 2020 Jan-Jun;14(1):63-66. doi: 10.4103/ajts.AJTS_98_19. Epub 2020 Jul 24.
Passenger lymphocyte syndrome (PLS), a subtype of graft-versus-host disease, is due to the production of antibodies by the donor "passenger" B lymphocytes against recipient's red cells. It is a rare disorder encountered mostly in ABO blood group-mismatched solid organ transplantation. The present case report illustrates the clinical presentation and the mode of management of PLS in a bidirectional ABO-incompatible renal transplantation. A 43-year-old male diagnosed with chronic kidney disease Stage 5-D (diabetic nephropathy) Type-2 hypertension with ischemic heart disease underwent ABO bidirectional-mismatched renal transplantation. The blood group of the patient was B Rh D positive and that of the donor (patient's wife) was A Rh D positive. In the pretransplantation phase, immunoglobulin G anti-A titer was 64 by column agglutination method, which was subsequently brought down to 4 by therapeutic plasma exchange and immunosuppression. Good graft function was established in the posttransplantation phase, but a significant drop in the hemoglobin (Hb) was noted. A fall in Hb, peripheral smear findings suggestive of hemolysis, and direct antiglobulin test positivity along with raised lactate dehydrogenase suggested the diagnosis of PLS; the patient was managed successfully for the same by transfusion of O blood group packed red blood cell transfusion and immunosuppression. PLS is a rare but important cause of immune-mediated hemolytic anemia in ABO-mismatched transplants.
过客淋巴细胞综合征(PLS)是移植物抗宿主病的一种亚型,是由于供体“过客”B淋巴细胞产生针对受者红细胞的抗体所致。它是一种罕见的疾病,多见于ABO血型不相容的实体器官移植。本病例报告阐述了双向ABO不相容肾移植中PLS的临床表现及处理方式。一名43岁男性,诊断为5-D期慢性肾脏病(糖尿病肾病)、2型高血压伴缺血性心脏病,接受了ABO双向不相容肾移植。患者血型为B Rh D阳性,供体(患者妻子)血型为A Rh D阳性。移植前阶段,通过柱凝集法检测免疫球蛋白G抗A效价为64,随后通过治疗性血浆置换和免疫抑制将其降至4。移植后阶段移植肾功能良好,但血红蛋白(Hb)显著下降。Hb下降、外周血涂片结果提示溶血、直接抗球蛋白试验阳性以及乳酸脱氢酶升高提示PLS诊断;通过输注O型浓缩红细胞和免疫抑制对患者进行了成功治疗。PLS是ABO不相容移植中免疫介导的溶血性贫血的一种罕见但重要的病因。