TY - JOUR
T1 - Integrating oral immunotherapy into clinical practice
AU - Leonard, Stephanie A.
AU - Laubach, Susan
AU - Wang, Julie
N1 - Funding Information:
Disclosure of Significant Relationships with Relevant Commercial Companies/Organizations: S. A. Leonard and S. Laubach receive research support from Aimmune Therapeutics and DBV Technologies. They have no financial disclosures pertaining to this article. S. A. Leonard is a Medical Advisory Board member for the International FPIES Association. J. Wang receives research support from the National Institute of Allergy and Infectious Diseases, Aimmune, DBV Technologies, and Regeneron, and has received consultancy fees from ALK Abello, DBV Technologies, and Genentech. Z. K. Ballas (editor) disclosed no relevant financial relationships.
Publisher Copyright:
© 2020
PY - 2021/1
Y1 - 2021/1
N2 - In 2020, the first food allergy treatment, an oral immunotherapy (OIT) product for peanut allergy, was approved by the Food and Drug Administration, and a peanut epicutaneous immunotherapy patch was under review. As food allergy therapies become available and widespread, allergy offices will need to adjust practices to be able to offer their patients these new treatments. OIT is an intensive therapy that requires commitment from patients and their families, and open communication with the practice is paramount. OIT may not be the right therapy for every patient, and although identifying good candidates is still an area rich for research opportunity, experience from cohorts and clinical trials provides some insight. It is important to understand the scope of practice for each member of the OIT team based on state regulations for a particular location. Staffing and space will likely dictate how many patients at an individual office could be on active OIT at one time. Emergency medications, supplies, and protocols must be in place. Screening, scheduling, visit procedures, monitoring, home dosing, dose modifications, safety precautions, adverse reactions, and maintenance will be addressed in this article. Finally, adjunct therapies under investigation will be reviewed.
AB - In 2020, the first food allergy treatment, an oral immunotherapy (OIT) product for peanut allergy, was approved by the Food and Drug Administration, and a peanut epicutaneous immunotherapy patch was under review. As food allergy therapies become available and widespread, allergy offices will need to adjust practices to be able to offer their patients these new treatments. OIT is an intensive therapy that requires commitment from patients and their families, and open communication with the practice is paramount. OIT may not be the right therapy for every patient, and although identifying good candidates is still an area rich for research opportunity, experience from cohorts and clinical trials provides some insight. It is important to understand the scope of practice for each member of the OIT team based on state regulations for a particular location. Staffing and space will likely dictate how many patients at an individual office could be on active OIT at one time. Emergency medications, supplies, and protocols must be in place. Screening, scheduling, visit procedures, monitoring, home dosing, dose modifications, safety precautions, adverse reactions, and maintenance will be addressed in this article. Finally, adjunct therapies under investigation will be reviewed.
KW - Oral immunotherapy
KW - epicutaneous immunotherapy
KW - food allergy treatment
KW - sublingual immunotherapy
UR - http://www.scopus.com/inward/record.url?scp=85099199378&partnerID=8YFLogxK
U2 - 10.1016/j.jaci.2020.11.011
DO - 10.1016/j.jaci.2020.11.011
M3 - Review article
C2 - 33436161
AN - SCOPUS:85099199378
SN - 0091-6749
VL - 147
SP - 1
EP - 13
JO - Journal of Allergy and Clinical Immunology
JF - Journal of Allergy and Clinical Immunology
IS - 1
ER -