Infection outcomes in patients with common variable immunodeficiency disorders: relationship to immunoglobulin therapy over 22 years.

BACKGROUND: Common variable immunodeficiency disorders (CVIDs) are the most common forms of symptomatic primary antibody failure in adults and children. Replacement immunoglobulin is the standard treatment, although there are few consistent data on optimal dosages and target trough IgG levels requi...

Olles dieđut

Bibliográfalaš dieđut
Váldodahkkit: Lucas, M, Lee, M, Lortan, J, Lopez-Granados, E, Misbah, S, Chapel, H
Materiálatiipa: Journal article
Giella:English
Almmustuhtton: 2010
_version_ 1826279740677292032
author Lucas, M
Lee, M
Lortan, J
Lopez-Granados, E
Misbah, S
Chapel, H
author_facet Lucas, M
Lee, M
Lortan, J
Lopez-Granados, E
Misbah, S
Chapel, H
author_sort Lucas, M
collection OXFORD
description BACKGROUND: Common variable immunodeficiency disorders (CVIDs) are the most common forms of symptomatic primary antibody failure in adults and children. Replacement immunoglobulin is the standard treatment, although there are few consistent data on optimal dosages and target trough IgG levels required for infection prevention. OBJECTIVE: To provide data to support the hypothesis that each patient requires an individual dose of therapeutic immunoglobulin to prevent breakthrough infections and that efficacious trough IgG levels vary between patients. METHODS: Data, collected prospectively from a cohort of 90 patients with confirmed CVIDs from 1 center over a follow-up period of 22 years, was validated and analyzed. Immunoglobulin doses had been adjusted in accordance with infections rather than to achieve a particular trough IgG level. Doses to achieve infection-free periods were determined and resultant trough levels analyzed. A smaller group of patients with X-linked agammaglobulinemia was analyzed for comparison. RESULTS: Patients with a CVID had a range of trough IgG levels that prevented breakthrough bacterial infections (5-17 g/L); viral and fungal infections were rare. Doses of replacement immunoglobulin to prevent breakthrough infections ranged from 0.2 to 1.2 g/kg/mo. Those with proven bronchiectasis or particular clinical phenotypes required higher replacement doses. Patients with X-linked agammaglobulinemia showed a similar range of IgG levels to stay infection-free (8-13 g/L). CONCLUSION: These data offer guidance regarding optimal doses and target trough IgG levels in individual patients with CVIDs with or without bronchiectasis and for particular clinical phenotypes. The goal of replacement therapy should be to improve clinical outcome and not to reach a particular IgG trough level.
first_indexed 2024-03-07T00:03:18Z
format Journal article
id oxford-uuid:76b5f846-7e5a-41b8-8ba9-7743fe8ed66c
institution University of Oxford
language English
last_indexed 2024-03-07T00:03:18Z
publishDate 2010
record_format dspace
spelling oxford-uuid:76b5f846-7e5a-41b8-8ba9-7743fe8ed66c2022-03-26T20:18:01ZInfection outcomes in patients with common variable immunodeficiency disorders: relationship to immunoglobulin therapy over 22 years.Journal articlehttp://purl.org/coar/resource_type/c_dcae04bcuuid:76b5f846-7e5a-41b8-8ba9-7743fe8ed66cEnglishSymplectic Elements at Oxford2010Lucas, MLee, MLortan, JLopez-Granados, EMisbah, SChapel, H BACKGROUND: Common variable immunodeficiency disorders (CVIDs) are the most common forms of symptomatic primary antibody failure in adults and children. Replacement immunoglobulin is the standard treatment, although there are few consistent data on optimal dosages and target trough IgG levels required for infection prevention. OBJECTIVE: To provide data to support the hypothesis that each patient requires an individual dose of therapeutic immunoglobulin to prevent breakthrough infections and that efficacious trough IgG levels vary between patients. METHODS: Data, collected prospectively from a cohort of 90 patients with confirmed CVIDs from 1 center over a follow-up period of 22 years, was validated and analyzed. Immunoglobulin doses had been adjusted in accordance with infections rather than to achieve a particular trough IgG level. Doses to achieve infection-free periods were determined and resultant trough levels analyzed. A smaller group of patients with X-linked agammaglobulinemia was analyzed for comparison. RESULTS: Patients with a CVID had a range of trough IgG levels that prevented breakthrough bacterial infections (5-17 g/L); viral and fungal infections were rare. Doses of replacement immunoglobulin to prevent breakthrough infections ranged from 0.2 to 1.2 g/kg/mo. Those with proven bronchiectasis or particular clinical phenotypes required higher replacement doses. Patients with X-linked agammaglobulinemia showed a similar range of IgG levels to stay infection-free (8-13 g/L). CONCLUSION: These data offer guidance regarding optimal doses and target trough IgG levels in individual patients with CVIDs with or without bronchiectasis and for particular clinical phenotypes. The goal of replacement therapy should be to improve clinical outcome and not to reach a particular IgG trough level.
spellingShingle Lucas, M
Lee, M
Lortan, J
Lopez-Granados, E
Misbah, S
Chapel, H
Infection outcomes in patients with common variable immunodeficiency disorders: relationship to immunoglobulin therapy over 22 years.
title Infection outcomes in patients with common variable immunodeficiency disorders: relationship to immunoglobulin therapy over 22 years.
title_full Infection outcomes in patients with common variable immunodeficiency disorders: relationship to immunoglobulin therapy over 22 years.
title_fullStr Infection outcomes in patients with common variable immunodeficiency disorders: relationship to immunoglobulin therapy over 22 years.
title_full_unstemmed Infection outcomes in patients with common variable immunodeficiency disorders: relationship to immunoglobulin therapy over 22 years.
title_short Infection outcomes in patients with common variable immunodeficiency disorders: relationship to immunoglobulin therapy over 22 years.
title_sort infection outcomes in patients with common variable immunodeficiency disorders relationship to immunoglobulin therapy over 22 years
work_keys_str_mv AT lucasm infectionoutcomesinpatientswithcommonvariableimmunodeficiencydisordersrelationshiptoimmunoglobulintherapyover22years
AT leem infectionoutcomesinpatientswithcommonvariableimmunodeficiencydisordersrelationshiptoimmunoglobulintherapyover22years
AT lortanj infectionoutcomesinpatientswithcommonvariableimmunodeficiencydisordersrelationshiptoimmunoglobulintherapyover22years
AT lopezgranadose infectionoutcomesinpatientswithcommonvariableimmunodeficiencydisordersrelationshiptoimmunoglobulintherapyover22years
AT misbahs infectionoutcomesinpatientswithcommonvariableimmunodeficiencydisordersrelationshiptoimmunoglobulintherapyover22years
AT chapelh infectionoutcomesinpatientswithcommonvariableimmunodeficiencydisordersrelationshiptoimmunoglobulintherapyover22years