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Sökning: WFRF:(Lundkvist A) > (2020-2023) > High dose pollen in...

High dose pollen intralymphatic immunotherapy: Two RDBPC trials question the benefit of dose increase

Hellkvist, L. (författare)
Karolinska Institute,Karolinska Institutet,Karolinska University Hospital
Hjalmarsson, E. (författare)
Karolinska Institute,Karolinska Institutet
Weinfeld, D. (författare)
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Dahl, Åslög, 1955 (författare)
University of Gothenburg,Gothenburg University,Göteborgs universitet,Institutionen för biologi och miljövetenskap,Department of Biological and Environmental Sciences
Karlsson, A. (författare)
Karolinska Institute,Karolinska University Hospital
Westman, M. (författare)
Karolinska Institute
Lundkvist, K. (författare)
Karolinska Institute
Winqvist, O. (författare)
Karolinska Institute
Georen, S. K. (författare)
Karolinska Institute,Karolinska Institutet
Westin, Ulla (författare)
Lund University,Lunds universitet,Laryngoesofagologi, allergi och livskvalitet,Forskargrupper vid Lunds universitet,Laryngoesophagology, Allergy and Life Quality,Lund University Research Groups,Skåne University Hospital
Cardell, L. O. (författare)
Karolinska Institute,Karolinska Institutet,Karolinska University Hospital
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 (creator_code:org_t)
2021-08-29
2022
Engelska.
Ingår i: Allergy. - : Wiley. - 0105-4538 .- 1398-9995. ; 77:3, s. 883-96
  • Tidskriftsartikel (refereegranskat)
Abstract Ämnesord
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  • Background The same dosing schedule, 1000 SQ-U times three, with one-month intervals, have been evaluated in most trials of intralymphatic immunotherapy (ILIT) for the treatment of allergic rhinitis (AR). The present studies evaluated if a dose escalation in ILIT can enhance the clinical and immunological effects, without compromising safety. Methods Two randomized double-blind placebo-controlled trials of ILIT for grass pollen-induced AR were performed. The first included 29 patients that had recently ended 3 years of SCIT and the second contained 39 not previously vaccinated patients. An up-dosage of 1000-3000-10,000 (5000 + 5000 with 30 minutes apart) SQ-U with 1 month in between was evaluated. Results Doses up to 10,000 SQ-U were safe after recent SCIT. The combined symptom-medication scores (CSMS) were reduced by 31% and the grass-specific IgG4 levels in blood were doubled. In ILIT de novo, the two first patients that received active treatment developed serious adverse reactions at 5000 SQ-U. A modified up-dosing schedule; 1000-3000-3000 SQ-U appeared to be safe but failed to improve the CSMS. Flow cytometry analyses showed increased activation of lymph node-derived dendritic but not T cells. Quality of life and nasal provocation response did not improve in any study. Conclusion Intralymphatic immunotherapy in high doses after SCIT appears to further reduce grass pollen-induced seasonal symptoms and may be considered as an add-on treatment for patients that do not reach full symptom control after SCIT. Up-dosing schedules de novo with three monthly injections that exceeds 3000 SQ-U should be avoided.

Ämnesord

MEDICIN OCH HÄLSOVETENSKAP  -- Medicinska och farmaceutiska grundvetenskaper -- Immunologi inom det medicinska området (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Basic Medicine -- Immunology in the medical area (hsv//eng)
MEDICIN OCH HÄLSOVETENSKAP  -- Klinisk medicin -- Lungmedicin och allergi (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Clinical Medicine -- Respiratory Medicine and Allergy (hsv//eng)

Nyckelord

clinical immunology
immunotherapy and tolerance induction
pollen
rhinitis
allergen-specific immunotherapy
recombinant allergens
young-adults
clinical-use
efficacy
route
rhinoconjunctivitis
injections
rhinitis
asthma
Allergy
Immunology

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