TY - JOUR
T1 - Novel Approaches to Treatment of Immune-Mediated Chronic Intestinal Pseudo-Obstruction
AU - Vilaseca, Andreu
AU - Arranz, Paula
AU - Llaurado, Arnau
AU - Zabalza, Ana
AU - Fonseca, Elianet Gisell
AU - Medina, Inmaculada
AU - Gómez Lorente, Maria Amelia
AU - Alcalá-González, Luis
AU - Borruel, Natalia
AU - Fernández-Forcelledo, José Luis
AU - Ariño, Helena
AU - Armangue, Thais
AU - Montalban, Xavier
AU - Graus, Francesc
AU - Malagelada, Carolina
PY - 2025/3
Y1 - 2025/3
N2 - BACKGROUND AND OBJECTIVES: The optimal immunosuppressive treatment for autoimmune chronic intestinal pseudo-obstruction (CIPO) is unknown due to lack of clinical trials. Even less data exist on treatment recommendations for patients who do not respond to first-line immunotherapy.METHODS: We describe 4 patients with autoimmune CIPO treated with vedolizumab (3/4), a monoclonal antibody that interferes the lymphocyte trafficking to the gastrointestinal tract, or rituximab (1/4) who did not respond to steroids or IV immunoglobulins. We made a systematic review of previously published cases of CIPO treated with these biological agents.RESULTS: Vedolizumab was effective in 2 of 3 patients but failed in a child with nonparaneoplastic anti-Hu-associated CIPO, who had generalized dysautonomia. The 2 patients who responded to vedolizumab had an isolated CIPO, and they did not present neuronal antibodies. Rituximab was prescribed in a case of anti-Hu-associated, nonparaneoplastic CIPO, who showed a complete clinical response after this treatment. Our review of the literature retrieved 4 previous cases of autoimmune CIPO treated with rituximab but none treated with vedolizumab. All patients treated with rituximab had Hu antibodies. Two patients showed a clinical response to the treatment with rituximab.DISCUSSION: Our findings underscore the potential efficacy of rituximab and vedolizumab in the management of autoimmune CIPO refractory to first-line treatments.
AB - BACKGROUND AND OBJECTIVES: The optimal immunosuppressive treatment for autoimmune chronic intestinal pseudo-obstruction (CIPO) is unknown due to lack of clinical trials. Even less data exist on treatment recommendations for patients who do not respond to first-line immunotherapy.METHODS: We describe 4 patients with autoimmune CIPO treated with vedolizumab (3/4), a monoclonal antibody that interferes the lymphocyte trafficking to the gastrointestinal tract, or rituximab (1/4) who did not respond to steroids or IV immunoglobulins. We made a systematic review of previously published cases of CIPO treated with these biological agents.RESULTS: Vedolizumab was effective in 2 of 3 patients but failed in a child with nonparaneoplastic anti-Hu-associated CIPO, who had generalized dysautonomia. The 2 patients who responded to vedolizumab had an isolated CIPO, and they did not present neuronal antibodies. Rituximab was prescribed in a case of anti-Hu-associated, nonparaneoplastic CIPO, who showed a complete clinical response after this treatment. Our review of the literature retrieved 4 previous cases of autoimmune CIPO treated with rituximab but none treated with vedolizumab. All patients treated with rituximab had Hu antibodies. Two patients showed a clinical response to the treatment with rituximab.DISCUSSION: Our findings underscore the potential efficacy of rituximab and vedolizumab in the management of autoimmune CIPO refractory to first-line treatments.
KW - Humans
KW - Intestinal Pseudo-Obstruction/drug therapy
KW - Antibodies, Monoclonal, Humanized/therapeutic use
KW - Male
KW - Female
KW - Rituximab/therapeutic use
KW - Gastrointestinal Agents/therapeutic use
KW - Autoimmune Diseases/drug therapy
KW - Chronic Disease
KW - Child
KW - Adult
KW - Immunologic Factors/pharmacology
KW - Adolescent
UR - https://portalrecerca.uab.cat/es/publications/novel-approaches-to-treatment-of-immune-mediated-chronic-intestin
UR - http://www.scopus.com/inward/record.url?scp=85217525322&partnerID=8YFLogxK
U2 - 10.1212/NXI.0000000000200369
DO - 10.1212/NXI.0000000000200369
M3 - Article
C2 - 39908479
SN - 2332-7812
VL - 12
JO - Neurology(R) neuroimmunology & neuroinflammation
JF - Neurology(R) neuroimmunology & neuroinflammation
IS - 2
M1 - e200369
ER -