TY - JOUR
T1 - Application of enzyme-linked immunosorbent assay to detect antimicrobial peptides in human intestinal lumen
AU - Hong, Julie S.
AU - Shamim, Abrar
AU - Atta, Hussein
AU - Nonnecke, Eric B.
AU - Merl, Sarah
AU - Patwardhan, Satyajit
AU - Manell, Elin
AU - Gunes, Esad
AU - Jordache, Philip
AU - Chen, Bryan
AU - Lu, Wuyuan
AU - Shen, Bo
AU - Dionigi, Beatrice
AU - Kiran, Ravi P.
AU - Sykes, Megan
AU - Zorn, Emmanuel
AU - Bevins, Charles L.
AU - Weiner, Joshua
PY - 2024
Y1 - 2024
N2 - Intestinal transplantation is the definitive treatment for intestinal failure. However, tissue rejection and graft versus-host disease are relatively common complications, necessitating aggressive immunosuppression that can itself pose further complications. Tracking intraluminal markers in ileal effluent from standard ileostomies may present a noninvasive and sensitive way to detect developing pathology within the intestinal graft. This would be an improvement compared to current assessments, which are limited by poor sensitivity and specificity, contributing to under or over-immunosuppression, respectively, and by the need for invasive biopsies. Herein, we report an approach to reproducibly analyze ileal fluid obtained through stoma sampling for antimicrobial peptide/protein concentrations, reasoning that these molecules may provide an assessment of intestinal homeostasis and levels of intestinal inflammation over time. Concentrations of lysozyme (LYZ), myeloperoxidase (MPO), calprotectin (S100A8/A9) and beta-defensin 2 (DEFB2) were assessed using adaptations of commercially available enzyme-linked immunosorbent assays (ELISAs). The concentration of alpha-defensin 5 (DEFA5) was assessed using a newly developed sandwich ELISA. Our data support that with proper preparation of ileal effluent specimens, precise and replicable determination of antimicrobial peptide/protein concentrations can be achieved for each of these target molecules via ELISA. This approach may prove to be reliable as a clinically useful assessment of intestinal homeostasis over time for patients with ileostomies.
AB - Intestinal transplantation is the definitive treatment for intestinal failure. However, tissue rejection and graft versus-host disease are relatively common complications, necessitating aggressive immunosuppression that can itself pose further complications. Tracking intraluminal markers in ileal effluent from standard ileostomies may present a noninvasive and sensitive way to detect developing pathology within the intestinal graft. This would be an improvement compared to current assessments, which are limited by poor sensitivity and specificity, contributing to under or over-immunosuppression, respectively, and by the need for invasive biopsies. Herein, we report an approach to reproducibly analyze ileal fluid obtained through stoma sampling for antimicrobial peptide/protein concentrations, reasoning that these molecules may provide an assessment of intestinal homeostasis and levels of intestinal inflammation over time. Concentrations of lysozyme (LYZ), myeloperoxidase (MPO), calprotectin (S100A8/A9) and beta-defensin 2 (DEFB2) were assessed using adaptations of commercially available enzyme-linked immunosorbent assays (ELISAs). The concentration of alpha-defensin 5 (DEFA5) was assessed using a newly developed sandwich ELISA. Our data support that with proper preparation of ileal effluent specimens, precise and replicable determination of antimicrobial peptide/protein concentrations can be achieved for each of these target molecules via ELISA. This approach may prove to be reliable as a clinically useful assessment of intestinal homeostasis over time for patients with ileostomies.
KW - Intestinal transplantation
KW - Transplantation immunology
KW - ELISA
KW - Methods
KW - Crohn 's disease
KW - Intestinal transplantation
KW - Transplantation immunology
KW - ELISA
KW - Methods
KW - Crohn 's disease
UR - https://res.slu.se/id/publ/128208
U2 - 10.1016/j.jim.2023.113599
DO - 10.1016/j.jim.2023.113599
M3 - Journal article
C2 - 38081407
SN - 0022-1759
VL - 525
JO - Journal of Immunological Methods
JF - Journal of Immunological Methods
M1 - 113599
ER -