A novel immunocomplex capture fluorescence assay (ICFA) using fluorescent beads and transfected cells for specific identification of human neutrophil antigen (HNA)‐1a and ‐1b antibodies

Fuente: Wiley Open Access
Salvato in:
Dettagli Bibliografici
Autori principali: Hiromi Kamada, Daisuke Takahashi, Marie Shimizu, Miyuki Uchida, Yoshihisa Watanabe, Fumiaki Nakajima, Shigeki Miyata, Masahiro Satake
Natura: Artículo Open Access
Pubblicazione: Wiley 2024
Soggetti:
Accesso online:
Tags: Aggiungi Tag
Nessun Tag, puoi essere il primo ad aggiungerne!!
_version_ 1867002698050568192
author Hiromi Kamada
Daisuke Takahashi
Marie Shimizu
Miyuki Uchida
Yoshihisa Watanabe
Fumiaki Nakajima
Shigeki Miyata
Masahiro Satake
author_facet Hiromi Kamada
Daisuke Takahashi
Marie Shimizu
Miyuki Uchida
Yoshihisa Watanabe
Fumiaki Nakajima
Shigeki Miyata
Masahiro Satake
Hiromi Kamada
Daisuke Takahashi
Marie Shimizu
Miyuki Uchida
Yoshihisa Watanabe
Fumiaki Nakajima
Shigeki Miyata
Masahiro Satake
collection Wiley Open Access
contents A novel immunocomplex capture fluorescence assay (ICFA) using fluorescent beads and transfected cells for specific identification of human neutrophil antigen (HNA)‐1a and ‐1b antibodies Hiromi Kamada Daisuke Takahashi Marie Shimizu Miyuki Uchida Yoshihisa Watanabe Fumiaki Nakajima Shigeki Miyata Masahiro Satake Transfusion AbstractBackgroundTo identify specific human neutrophil antigen (HNA) antibodies, assays using neutrophils such as monoclonal antibody‐specific immobilization of granulocyte antigens (MAIGA) are recommended. However, these assays are limited by labor‐intensive neutrophil preparation and varying antigen expression levels.MethodsWe evaluated a newly developed immunocomplex capture fluorescence assay (ICFA) for identifying HNA‐1 antibodies and compared it to MAIGA and LABScreen Multi (LABM), which utilizes recombinant HNA‐coated Luminex beads. For ICFA, HNA‐1a or HNA‐1b transfected cells replaced neutrophils. Cells incubated with serum were lysed, and immune complexes were captured using five CD16 monoclonal antibody‐conjugated Luminex beads. Nine antisera with known specificity and 26 samples suspected of containing HNA antibodies were analyzed by ICFA and MAIGA using neutrophils or transfected cells (ICFA‐N or ICFA‐T, and MAIGA‐N or MAIGA‐T, respectively).ResultsICFA‐T and MAIGA‐N accurately determined the specificity of all antibodies in the nine antiserum samples. The ICFA‐T detection limit was 2048‐fold for anti–HNA‐1a and 256‐fold for anti‐HNA‐1b; the limits of MAIGA‐T, MAIGA‐N, and LABM were 32‐, 4 ~ 64‐, and 128‐fold for anti‐HNA‐1a and 64‐, 16 ~ 64‐, and 32‐fold for anti–HNA‐1b, respectively. Twelve and 7 of the remaining 26 samples tested negative and positive, respectively, in both ICFA‐T and MAIGA‐N. Antibody specificity against HNA‐1a or HNA‐1b determined using ICFA‐T agreed with that determined using MAIGA‐N and LABM. Another seven samples tested positive in ICFA‐T but negative in MAIGA‐N.ConclusionThe novel ICFA is highly sensitive and exhibits specificity similar to MAIGA and LABM for detecting HNA‐1 antibodies. 10.1111/trf.17813 http://onlinelibrary.wiley.com/termsAndConditions#vor
doi_str_mv 10.1111/trf.17813
format Artículo Open Access
id wiley_oa_10_1111_trf_17813
institution Wiley Open Access
license_str_mv http://onlinelibrary.wiley.com/termsAndConditions#vor
publishDate 2024
publisher Wiley
record_format wiley_oa
spellingShingle A novel immunocomplex capture fluorescence assay (ICFA) using fluorescent beads and transfected cells for specific identification of human neutrophil antigen (HNA)‐1a and ‐1b antibodies
Hiromi Kamada
Daisuke Takahashi
Marie Shimizu
Miyuki Uchida
Yoshihisa Watanabe
Fumiaki Nakajima
Shigeki Miyata
Masahiro Satake
Transfusion
A novel immunocomplex capture fluorescence assay (ICFA) using fluorescent beads and transfected cells for specific identification of human neutrophil antigen (HNA)‐1a and ‐1b antibodies Hiromi Kamada Daisuke Takahashi Marie Shimizu Miyuki Uchida Yoshihisa Watanabe Fumiaki Nakajima Shigeki Miyata Masahiro Satake Transfusion AbstractBackgroundTo identify specific human neutrophil antigen (HNA) antibodies, assays using neutrophils such as monoclonal antibody‐specific immobilization of granulocyte antigens (MAIGA) are recommended. However, these assays are limited by labor‐intensive neutrophil preparation and varying antigen expression levels.MethodsWe evaluated a newly developed immunocomplex capture fluorescence assay (ICFA) for identifying HNA‐1 antibodies and compared it to MAIGA and LABScreen Multi (LABM), which utilizes recombinant HNA‐coated Luminex beads. For ICFA, HNA‐1a or HNA‐1b transfected cells replaced neutrophils. Cells incubated with serum were lysed, and immune complexes were captured using five CD16 monoclonal antibody‐conjugated Luminex beads. Nine antisera with known specificity and 26 samples suspected of containing HNA antibodies were analyzed by ICFA and MAIGA using neutrophils or transfected cells (ICFA‐N or ICFA‐T, and MAIGA‐N or MAIGA‐T, respectively).ResultsICFA‐T and MAIGA‐N accurately determined the specificity of all antibodies in the nine antiserum samples. The ICFA‐T detection limit was 2048‐fold for anti–HNA‐1a and 256‐fold for anti‐HNA‐1b; the limits of MAIGA‐T, MAIGA‐N, and LABM were 32‐, 4 ~ 64‐, and 128‐fold for anti‐HNA‐1a and 64‐, 16 ~ 64‐, and 32‐fold for anti–HNA‐1b, respectively. Twelve and 7 of the remaining 26 samples tested negative and positive, respectively, in both ICFA‐T and MAIGA‐N. Antibody specificity against HNA‐1a or HNA‐1b determined using ICFA‐T agreed with that determined using MAIGA‐N and LABM. Another seven samples tested positive in ICFA‐T but negative in MAIGA‐N.ConclusionThe novel ICFA is highly sensitive and exhibits specificity similar to MAIGA and LABM for detecting HNA‐1 antibodies. 10.1111/trf.17813 http://onlinelibrary.wiley.com/termsAndConditions#vor
title A novel immunocomplex capture fluorescence assay (ICFA) using fluorescent beads and transfected cells for specific identification of human neutrophil antigen (HNA)‐1a and ‐1b antibodies
topic Transfusion
url https://onlinelibrary.wiley.com/doi/10.1111/trf.17813