Transfusion-associated graft-versus-host disease

Transfusion-associated graft-versus-host disease (TA-GvHD) is a rare complication of blood transfusion, in which the immunologically competent donor T lymphocytes mount an immune response against the recipient's lymphoid tissue.[1] These donor lymphocytes engraft, recognize recipient cells as foreign and mount an immune response against recipient tissues.[2] Donor lymphocytes are usually identified as foreign and destroyed by the recipient's immune system. However, in situations where the recipient is severely immunocompromised, or when the donor and recipient HLA type is similar (as can occur in directed donations from first-degree relatives), the recipient's immune system is not able to destroy the donor lymphocytes. This can result in transfusion associated graft-versus-host disease. This is in contrast with organ/tissue transplant associated GvHD, where matching HLA reduces the incident of the complication.[3]

Transfusion-associated graft-versus-host-disease
Other namesTA-GvHD
SpecialtyHematology

Signs and symptoms

The clinical presentation is the same as GvHD occurring in other settings, such as bone marrow transplantation. TA-GvHD can develop two days to six weeks after the transfusion.[4] Typical symptoms include:[4]

Other symptoms can include cough, abdominal pain, dyspnea and vomiting.[5]

Diagnosis

Laboratory findings include pancytopenia, marrow aplasia, abnormal liver enzymes, and electrolyte imbalance (when diarrhea is present).

TA-GvHD can be suspected from a biopsy of the affected skin or liver,[4] and established by HLA analysis of the circulating lymphocytes. This testing can identify circulating lymphocytes with a different HLA type than the tissue cells of the host.

In 2023, the first case of fetal-induced GvHD was reported in the New England Journal of Medicine.[6]

Prevention

Prevention includes gamma irradiation of the lymphocyte-containing blood components such as red blood cells, platelets and granulocytes. Irradiated blood components should be issued in the following situations:[7]

  • Intrauterine transfusions
  • Prematurity, low birthweight, or erythroblastosis fetalis in newborns
  • Congenital immunodeficiencies
  • Certain hematologic malignancies (e.g. Hodgkin lymphoma)
  • Patients undergoing hematopoietic stem cell transplantation
  • Components that are HLA matched, or directed donations from a family member
  • Patients receiving fludarabine therapy
  • Patients receiving granulocyte transfusions

Treatment

Treatment is supportive. No available form of therapy has proven effective in treating TA-GvHD and it is fatal in more than 90% of cases.[2]

Epidemiology

The incidence of TA-GvHD in immunocompromised patients receiving blood transfusions is estimated to be 0.1–1.0%, and mortality around 80–90%. Mortality is higher in TA-GvHD than in GvHD associated with bone marrow transplantation, where the engrafted lymphoid cells in the bone marrow are of donor origin (in autotransplant) and therefore the immune reaction is not directed against them.

The most common causes of death in TA-GvHD are infections and hemorrhages secondary to pancytopenia and liver dysfunction.

References
  1. "Complications of Transfusion: Transfusion Medicine: Merck Manual Professional". Retrieved 2009-02-09.
  2. Savage WJ (June 2016). "Transfusion Reactions". Hematology/Oncology Clinics of North America. 30 (3): 619–634. doi:10.1016/j.hoc.2016.01.012. PMID 27113000.
  3. Vaillant AA, Modi P, Mohammadi O (2022). "Graft Versus Host Disease". StatPearls. Treasure Island (FL): StatPearls Publishing. PMID 30855823. Retrieved 2023-02-02.
  4. "National Healthcare Safety Network (NHSN)". www.cdc.gov. 2017-12-29. Retrieved 2018-09-18.
  5. Patel KK, Patel AK, Ranjan RR, Shah AP (September 2010). "Transfusion associated graft versus host disease following whole blood transfusion from an unrelated donor in an immunocompetent patient". Indian Journal of Hematology & Blood Transfusion. 26 (3): 92–95. doi:10.1007/s12288-010-0028-0. PMC 3002081. PMID 21886390.
  6. A Case of Fetal-Induced Graft-versus-Host Disease
  7. Fung MK, Grossman BJ, Hillyer CD, Westhoff CM (2014). Technical manual (18th ed.). Bethesda, Md.: American Association of Blood Banks. ISBN 978-1563958885. OCLC 881812415.

Further reading
This article is issued from Wikipedia. The text is licensed under Creative Commons - Attribution - Sharealike. Additional terms may apply for the media files.