PMID- 35171984 OWN - NLM STAT- MEDLINE DCOM- 20221003 LR - 20221019 IS - 1543-2165 (Electronic) IS - 0003-9985 (Linking) VI - 146 IP - 10 DP - 2022 Oct 1 TI - Use of Human Leukocyte Antigen (HLA)-Incompatible Platelet Units in HLA Platelet-Refractory Patients With Limited Number of or Low-Level HLA Donor-Specific Antibodies Results in Permissive Transfusions. PG - 1243-1251 LID - 10.5858/arpa.2021-0051-OA [doi] AB - CONTEXT.-: In human leukocyte antigen (HLA)-mediated alloimmune platelet refractoriness, HLA-incompatible platelets may produce adequate posttransfusion corrected count increment ("permissive transfusion") and increase the donor pool. OBJECTIVE.-: To determine if a lower number of or low-level anti-HLA donor-specific antibodies (DSAs) predict permissive transfusion and could be used to prioritize platelet selection. DESIGN.-: We categorized platelets administered from 2016 to 2018 as HLA-compatible or HLA-incompatible based on presence of DSAs against the donor unit. We further divided HLA-incompatible units based on the number of DSAs and the level of DSAs (measured by mean fluorescence intensity [MFI]), where cumulative MFI >/=6000 defines high-level DSA. We compared posttransfusion corrected count increments (CCIs) and transfusion reactions among these transfusions. RESULTS.-: Of 279 HLA-selected units transfused into 26 platelet-refractory patients, we resorted to using 39 HLA-incompatible units (14%). Posttransfusion CCI and transfusion reaction frequency were similar among units targeted by 1 or low-level DSAs and HLA-compatible units. Units targeted by >/=2 distinct or high-level DSAs produced lower CCIs. Regardless of ABO compatibility, similarly HLA-categorized units yielded comparable CCIs and comparable frequency of transfusion reactions. CONCLUSIONS.-: HLA-incompatible platelets transfused across 1 or low-level DSAs were commonly permissive, whereas those transfused across >/=2 DSAs or high levels of DSA (MFI >/=6000) were nonpermissive. The use of such donor units offers transfusion services alternative platelet units for support of platelet-refractory patients. FAU - Sullivan, Jensyn Cone AU - Sullivan JC AD - From the Department of Pathology, Tufts Medical Center, Boston, Massachusetts (Cone Sullivan). FAU - Pena, Jeremy Ryan AU - Pena JR AD - From the Department of Pathology, Beth Israel Deaconess Medical Center, Boston, Massachusetts (Pena). LA - eng PT - Journal Article PL - United States TA - Arch Pathol Lab Med JT - Archives of pathology & laboratory medicine JID - 7607091 RN - 0 (Antibodies) RN - 0 (HLA Antigens) SB - IM MH - Antibodies MH - Blood Platelets MH - HLA Antigens MH - Humans MH - *Platelet Transfusion MH - Tissue Donors MH - *Transfusion Reaction EDAT- 2022/02/17 06:00 MHDA- 2022/10/04 06:00 CRDT- 2022/02/16 17:12 PHST- 2021/09/27 00:00 [accepted] PHST- 2022/02/17 06:00 [pubmed] PHST- 2022/10/04 06:00 [medline] PHST- 2022/02/16 17:12 [entrez] AID - 477900 [pii] AID - 10.5858/arpa.2021-0051-OA [doi] PST - ppublish SO - Arch Pathol Lab Med. 2022 Oct 1;146(10):1243-1251. doi: 10.5858/arpa.2021-0051-OA.