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  1. Article: Use of low-dose tacrolimus and associated hypomagnesemia in the prevention of erectile dysfunction following prostatectomy for prostate cancer.

    First, Martin R / Henning, Alice K / Fitzsimmons, William E

    Pharmacological reports : PR

    2016  Volume 68, Issue 6, Page(s) 1154–1158

    Abstract: Background: Hypomagnesemia with urinary magnesium wasting is a well described adverse event with calcineurin inhibitor therapy. Prostate cancer is the most prevalent cancer in men in the United States. Injury to the cavernous nerves during radical ... ...

    Abstract Background: Hypomagnesemia with urinary magnesium wasting is a well described adverse event with calcineurin inhibitor therapy. Prostate cancer is the most prevalent cancer in men in the United States. Injury to the cavernous nerves during radical prostatectomy frequently results in erectile dysfunction. Tacrolimus has been shown to be neuroprotective in the rat cavernous nerve injury model, an animal model representative of the neural injury that occurs in humans at the time of radical prostatectomy.
    Methods: In a randomized, double-blind, placebo-controlled trial, the utility of tacrolimus was assessed for prevention of erectile dysfunction following bilateral nerve-sparing radical prostatectomy.
    Results: Low dose tacrolimus, associated with low trough levels, resulted in mild hypomagnesemia, which was an early and persistent finding. As early as one week after institution of therapy, mean and median serum magnesium levels were significantly lower in the tacrolimus arm as compared to the placebo arm (p<0.001 for both). While the mean and median levels were within the normal range at Week 1, 10.9% of tacrolimus-treated patients had levels <1.8mg/dL, compared to none in the placebo arm (p=0.017). Median and mean levels remained significantly different at Week 5, Month 3 and Month 6. No clinical manifestations of hypomagnesemia were noted and no subject required treatment with magnesium. Changes in serum magnesium occurred earlier than other potential metabolic adverse events described with tacrolimus (changes in serum glucose, creatinine or potassium).
    Conclusions: These data indicate that mild hypomagnesemia is an early and sensitive biomarker for the effect of tacrolimus on the kidney.
    MeSH term(s) Calcineurin Inhibitors/administration & dosage ; Calcineurin Inhibitors/adverse effects ; Double-Blind Method ; Erectile Dysfunction/blood ; Erectile Dysfunction/diagnosis ; Erectile Dysfunction/prevention & control ; Humans ; Magnesium/blood ; Male ; Middle Aged ; Prostatectomy/adverse effects ; Prostatectomy/trends ; Prostatic Neoplasms/blood ; Prostatic Neoplasms/diagnosis ; Prostatic Neoplasms/therapy ; Tacrolimus/administration & dosage ; Tacrolimus/adverse effects
    Chemical Substances Calcineurin Inhibitors ; Magnesium (I38ZP9992A) ; Tacrolimus (WM0HAQ4WNM)
    Language English
    Publishing date 2016-07-30
    Publishing country Switzerland
    Document type Journal Article ; Multicenter Study ; Randomized Controlled Trial
    ZDB-ID 2186248-5
    ISSN 1734-1140
    ISSN 1734-1140
    DOI 10.1016/j.pharep.2016.07.009
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  2. Article ; Online: A Randomized, Double-Blind, Placebo-Controlled Trial to Assess the Utility of Tacrolimus (FK506) for the Prevention of Erectile Dysfunction Following Bilateral Nerve-Sparing Radical Prostatectomy.

    Mulhall, John P / Klein, Eric A / Slawin, Kevin / Henning, Alice K / Scardino, Peter T

    The journal of sexual medicine

    2018  Volume 15, Issue 9, Page(s) 1293–1299

    Abstract: Introduction: Radical prostatectomy (RP) is associated with erectile dysfunction, largely mediated through cavernous nerve injury. There are robust pre-clinical data supporting a potential role for neuromodulatory agents in this patient population. This ...

    Abstract Introduction: Radical prostatectomy (RP) is associated with erectile dysfunction, largely mediated through cavernous nerve injury. There are robust pre-clinical data supporting a potential role for neuromodulatory agents in this patient population. This study assessed tacrolimus in improving erectile function recovery rates after RP (ClinicalTrials.gov number, NCT00106392).
    Aim: To define the utility of oral tacrolimus in improving erectile function recovery after nerve sparing radical prostatectomy.
    Methods: A randomized, double-blind trial compared tacrolimus 2-3 mg daily and placebo in men undergoing RP. Patients had localized prostate cancer and excellent baseline erectile function, underwent bilateral nerve-sparing RP, and were followed up for at least 18 months after RP. Patients received study drug for 27 weeks and completed the International Index of Erectile Function erectile function domain (EFD) questionnaire at baseline and serially after surgery.
    Main outcome measures: International Index of Erectile Function erectile function domain score.
    Results: Data were available for 124 patients (59 tacrolimus, 65 placebo); mean age was 54.6 ± 6.2 years. No patient experienced permanent creatinine or potassium elevation. At baseline, mean EFD scores were 28.6 ± 2.1 (tacrolimus group) and 29 ± 1.5 (placebo group). By week 5, mean EFD scores had dropped to 8 ± 9.4 (tacrolimus) and 9 ± 10.7 (placebo). At 18 months, mean EFD scores were 16.0 ± 11.3 (tacrolimus) and 20.2 ± 9.0 (placebo) (P = .09). Tacrolimus failed to meet significance (hazard ratio = 0.83; P = .50), with no difference in: (i) percentage of patients achieving normal spontaneous erectile function (EFD score ≥24), (ii) time to normalization of EFD score (≥24), (iii) percentage of patients capable of intercourse in response to phosphieserase type 5 inhibitor (PDE5i), and (iv) time to achieve response to PDE5i.
    Clinical implications: Despite positive animal data, oral tacrolimus as used in this trial failed to improve erectile function after nerve sparing radical prostatectomy.
    Strengths & limitations: The study is limited by a high attrition rate. The strengths include a randomized, placebo controlled design, extensive patient monitoring, use of medication diaries and a validated instrument as the primary outcome measure.
    Conclusion: Despite supportive animal data, tacrolimus used in this fashion in the RP population failed to demonstrate any superiority over placebo. Mulhall JP, Klein EA, Slawin K, et al. A Randomized, Double-Blind, Placebo-Controlled Trial to Assess the Utility of Tacrolimus (FK506) for the Prevention of Erectile Dysfunction Following Bilateral Nerve-Sparing Radical Prostatectomy. J Sex Med 2018;15:1293-1299.
    MeSH term(s) Aged ; Double-Blind Method ; Erectile Dysfunction/drug therapy ; Humans ; Male ; Middle Aged ; Neurotransmitter Agents/administration & dosage ; Neurotransmitter Agents/therapeutic use ; Penile Erection ; Postoperative Complications/drug therapy ; Prostatectomy/adverse effects ; Prostatic Neoplasms/surgery ; Recovery of Function ; Surveys and Questionnaires ; Tacrolimus/administration & dosage ; Tacrolimus/therapeutic use ; Treatment Outcome ; United States
    Chemical Substances Neurotransmitter Agents ; Tacrolimus (WM0HAQ4WNM)
    Language English
    Publishing date 2018-09-06
    Publishing country Netherlands
    Document type Journal Article ; Multicenter Study ; Randomized Controlled Trial ; Research Support, Non-U.S. Gov't
    ZDB-ID 2251959-2
    ISSN 1743-6109 ; 1743-6095
    ISSN (online) 1743-6109
    ISSN 1743-6095
    DOI 10.1016/j.jsxm.2018.07.009
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  3. Article ; Online: Bayesian hierarchical evaluation of dose-response for peanut allergy in clinical trial screening.

    Haber, Lynne T / Reichard, John F / Henning, Alice K / Dawson, Peter / Chinthrajah, R Sharon / Sindher, Sayantani B / Long, Andrew / Vincent, Melissa J / Nadeau, Kari C / Allen, Bruce C

    Food and chemical toxicology : an international journal published for the British Industrial Biological Research Association

    2021  Volume 151, Page(s) 112125

    Abstract: Risk-based labeling based on the minimal eliciting doses (EDs) in sensitized populations is a potential replacement for precautionary allergen labeling of food allergens. We estimated the dose-response distribution for peanut allergen using data from ... ...

    Abstract Risk-based labeling based on the minimal eliciting doses (EDs) in sensitized populations is a potential replacement for precautionary allergen labeling of food allergens. We estimated the dose-response distribution for peanut allergen using data from double-blind placebo-controlled food challenges (DBPCFCs) conducted in the US at multiple sites, testing a population believed to be similar to the general U.S. food allergic population. Our final (placebo-adjusted) dataset included 548 challenges of 481 subjects. Bayesian hierarchical analysis facilitated model fitting, and accounted for variability associated with various levels of data organization. The data are best described using a complex hierarchical structure that accounts for inter-individual variability and variability across study locations or substudies. Bayesian model averaging could simultaneously consider the fit of multiple models, but the Weibull model dominated so strongly that model averaging was not needed. The ED01 and ED05 (and 95% credible intervals) are 0.052 (0.021, 0.13) and 0.49 (0.22, 0.97) mg peanut protein, respectively. Accounting for challenges with severe reactions at the LOAEL, by using the dose prior to the LOAEL as the new LOAEL, the ED01 drops to 0.029 (0.014, 0.074) mg peanut protein. Our results could aid in establishing improved food labeling guidelines in the management of food allergies.
    MeSH term(s) Adolescent ; Adult ; Arachis/immunology ; Bayes Theorem ; Child ; Dose-Response Relationship, Drug ; Double-Blind Method ; Female ; Humans ; Male ; Peanut Hypersensitivity/etiology ; Placebos ; Young Adult
    Chemical Substances Placebos
    Language English
    Publishing date 2021-03-12
    Publishing country England
    Document type Journal Article
    ZDB-ID 782617-5
    ISSN 1873-6351 ; 0278-6915
    ISSN (online) 1873-6351
    ISSN 0278-6915
    DOI 10.1016/j.fct.2021.112125
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  4. Article ; Online: Multicenter, randomized, double-blind, placebo-controlled clinical trial of vital wheat gluten oral immunotherapy.

    Nowak-Węgrzyn, Anna / Wood, Robert A / Nadeau, Kari C / Pongracic, Jacqueline A / Henning, Alice K / Lindblad, Robert W / Beyer, Kirsten / Sampson, Hugh A

    The Journal of allergy and clinical immunology

    2018  Volume 143, Issue 2, Page(s) 651–661.e9

    Abstract: Background: Wheat is a common food allergen that can cause anaphylaxis.: Objective: We sought to determine the efficacy and safety of vital wheat gluten (VWG) oral immunotherapy (OIT).: Methods: After baseline double-blind, placebo-controlled food ...

    Abstract Background: Wheat is a common food allergen that can cause anaphylaxis.
    Objective: We sought to determine the efficacy and safety of vital wheat gluten (VWG) oral immunotherapy (OIT).
    Methods: After baseline double-blind, placebo-controlled food challenge (DBPCFC), 46 patients with wheat allergy (median age, 8.7 years; range, 4.2-22.3 years) were randomized 1:1 to low-dose VWG OIT or placebo, with biweekly escalation to 1445 mg of wheat protein (WP). After a year 1 DBPCFC, active subjects continued low-dose VWG OIT for another year and underwent a year 2 DBPCFC and, if passed, a subsequent off-therapy DBPCFC. Placebo-treated subjects crossed over to high-dose VWG OIT (maximum, 2748 mg of WP).
    Results: The median baseline successfully consumed dose (SCD) was 43 mg of WP in both groups. At year 1, 12 (52.2%) of 23 low-dose VWG OIT-treated and 0 (0%) of 23 placebo-treated subjects achieved the primary end point of an SCD of 4443 mg of WP or greater (P < .0001); median SCDs were 4443 and 143 mg, respectively. At year 2, 7 (30.4%) of 23 low-dose VWG OIT-treated subjects were desensitized to an SCD of 7443 mg of WP; 3 (13%) achieved sustained unresponsiveness 8 to 10 weeks off therapy. Among placebo-treated subjects who crossed over to high-dose VWG OIT, 12 (57.1%) of 21 were desensitized after 1 year (median SCD, 7443 mg of WP; nonsignificant vs low-dose VWG OIT). At year 1, skin prick test responses and wheat- and omega-5 gliadin-specific IgE levels did not differ between groups; the low-dose VWG OIT median specific IgG
    Conclusions: Low- and high-dose VWG OIT induced desensitization in about one half of the subjects after 1 year of treatment. Two years of low-dose VWG OIT resulted in 30% desensitization, and 13% had sustained unresponsiveness.
    MeSH term(s) Administration, Oral ; Adolescent ; Allergens/immunology ; Allergens/therapeutic use ; Anaphylaxis/immunology ; Anaphylaxis/prevention & control ; Child ; Child, Preschool ; Desensitization, Immunologic/methods ; Double-Blind Method ; Female ; Glutens/immunology ; Humans ; Immune Tolerance ; Male ; Placebos ; Treatment Outcome ; Triticum/immunology ; Wheat Hypersensitivity/immunology ; Wheat Hypersensitivity/therapy ; Young Adult
    Chemical Substances Allergens ; Placebos ; Glutens (8002-80-0)
    Language English
    Publishing date 2018-10-30
    Publishing country United States
    Document type Journal Article ; Multicenter Study ; Randomized Controlled Trial ; Research Support, Non-U.S. Gov't
    ZDB-ID 121011-7
    ISSN 1097-6825 ; 1085-8725 ; 0091-6749
    ISSN (online) 1097-6825 ; 1085-8725
    ISSN 0091-6749
    DOI 10.1016/j.jaci.2018.08.041
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  5. Article ; Online: Early epitope-specific IgE antibodies are predictive of childhood peanut allergy.

    Suprun, Maria / Sicherer, Scott H / Wood, Robert A / Jones, Stacie M / Leung, Donald Y M / Henning, Alice K / Dawson, Peter / Burks, A Wesley / Lindblad, Robert / Getts, Robert / Suárez-Fariñas, Mayte / Sampson, Hugh A

    The Journal of allergy and clinical immunology

    2020  Volume 146, Issue 5, Page(s) 1080–1088

    Abstract: Background: Peanut allergy is characterized by the development of IgE against peanut antigen.: Objective: We sought to evaluate the evolution of epitope-specific (es)IgE and esIgG: Methods: The end point was allergy status at age 4: Results: At ...

    Abstract Background: Peanut allergy is characterized by the development of IgE against peanut antigen.
    Objective: We sought to evaluate the evolution of epitope-specific (es)IgE and esIgG
    Methods: The end point was allergy status at age 4
    Results: At age 4
    Conclusions: Early epitope-specific plus peanut-specific IgE is predictive of allergy status at age 4
    MeSH term(s) Adolescent ; Algorithms ; Allergens/immunology ; Arachis/immunology ; Child ; Child, Preschool ; Cohort Studies ; Epitopes/immunology ; Female ; Follow-Up Studies ; Humans ; Immune Tolerance ; Immunoglobulin E/metabolism ; Immunoglobulin G/metabolism ; Infant ; Machine Learning ; Male ; Peanut Hypersensitivity/diagnosis ; Peanut Hypersensitivity/immunology ; Precision Medicine ; Predictive Value of Tests ; Prognosis ; Prospective Studies
    Chemical Substances Allergens ; Epitopes ; Immunoglobulin G ; Immunoglobulin E (37341-29-0)
    Language English
    Publishing date 2020-08-11
    Publishing country United States
    Document type Journal Article ; Research Support, N.I.H., Extramural ; Research Support, Non-U.S. Gov't
    ZDB-ID 121011-7
    ISSN 1097-6825 ; 1085-8725 ; 0091-6749
    ISSN (online) 1097-6825 ; 1085-8725
    ISSN 0091-6749
    DOI 10.1016/j.jaci.2020.08.005
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  6. Article ; Online: Allergen-specific T cells and clinical features of food allergy: Lessons from CoFAR immunotherapy cohorts.

    Berin, M Cecilia / Agashe, Charuta / Burks, A Wesley / Chiang, David / Davidson, Wendy F / Dawson, Peter / Grishin, Alexander / Henning, Alice K / Jones, Stacie M / Kim, Edwin H / Leung, Donald Y M / Masilamani, Madhan / Scurlock, Amy M / Sicherer, Scott H / Wood, Robert A / Sampson, Hugh A

    The Journal of allergy and clinical immunology

    2021  Volume 149, Issue 4, Page(s) 1373–1382.e12

    Abstract: Background: Allergen-specific IL-4: Objective: We examined the food allergen-specific T-cell response in participants of 2 food allergen immunotherapy trials to assess the relationship of the T-cell response to clinical phenotypes, including response ...

    Abstract Background: Allergen-specific IL-4
    Objective: We examined the food allergen-specific T-cell response in participants of 2 food allergen immunotherapy trials to assess the relationship of the T-cell response to clinical phenotypes, including response to immunotherapy.
    Methods: Blood was obtained from 84 participants with peanut allergy and 142 participants with egg allergy who underwent double-blind placebo-controlled food challenges. Peanut- and egg-responsive T cells were identified by CD154 upregulation after stimulation with the respective extract. Intracellular cytokines and chemokine receptors were also detected. The response to peanut epicutaneous immunotherapy (Peanut Epicutaneous Phase II Immunotherapy Clinical Trial [CoFAR6]; 49 participants receiving epicutaneous immunotherapy) and egg oral immunotherapy or a baked egg diet (Baked Egg or Egg Oral Immunotherapy for Children With Egg Allergy [CoFAR7]; 92 participants) was monitored over time.
    Results: Peanut-specific type 2 and CCR6
    Conclusion: Food-specific type 2 T cells at baseline are informative of threshold of reactivity and response to immunotherapy.
    MeSH term(s) Administration, Oral ; Allergens ; Arachis ; Desensitization, Immunologic ; Egg Hypersensitivity/therapy ; Food Hypersensitivity/therapy ; Humans ; Immunoglobulin E ; Immunologic Factors ; Peanut Hypersensitivity/therapy
    Chemical Substances Allergens ; Immunologic Factors ; Immunoglobulin E (37341-29-0)
    Language English
    Publishing date 2021-10-13
    Publishing country United States
    Document type Clinical Trial, Phase II ; Journal Article ; Randomized Controlled Trial ; Research Support, N.I.H., Extramural
    ZDB-ID 121011-7
    ISSN 1097-6825 ; 1085-8725 ; 0091-6749
    ISSN (online) 1097-6825 ; 1085-8725
    ISSN 0091-6749
    DOI 10.1016/j.jaci.2021.09.029
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  7. Article ; Online: Interleukin-2 receptor antagonist therapy leads to increased tacrolimus levels after kidney transplantation.

    Lin, Sonia / Henning, Alice K / Akhlaghi, Fatemeh / Reisfield, Robin / Vergara-Silva, Andrea / First, M Roy

    Therapeutic drug monitoring

    2015  Volume 37, Issue 2, Page(s) 206–213

    Abstract: Background: Tacrolimus (TAC) is a known substrate for cytochrome P450 (CYP) enzyme. CYP enzyme activity can be modulated by activation of IL-2 receptors (IL-2R) expressed on hepatocytes and intestinal cells. IL-2R antagonists (IL-2RA) may promote ... ...

    Abstract Background: Tacrolimus (TAC) is a known substrate for cytochrome P450 (CYP) enzyme. CYP enzyme activity can be modulated by activation of IL-2 receptors (IL-2R) expressed on hepatocytes and intestinal cells. IL-2R antagonists (IL-2RA) may promote preferential binding of circulating IL-2 to IL-2Rs on these cells by blocking IL-2Rs on activated T cells. This downregulates CYP enzymes, leading to increased calcineurin inhibitor levels. This analysis evaluates the significance of this drug-drug interaction in kidney transplant recipients.
    Methods: Data were used from a previous 5-year randomized, controlled study comparing outcomes associated with maintenance immunosuppression using 2 corticosteroid regimens: long-term therapy versus early withdrawal. Patients received either IL-2RAs or rabbit anti-thymocyte globulin (rATG) for induction. Serial TAC trough levels and doses were compared between induction agents within each corticosteroid arm. Rejection rates, patient/graft survival, and TAC adverse effects were also evaluated.
    Results: In the first week, IL-2RA-treated patients achieved significantly higher trough levels and required lower doses (in milligram per kilogram) to achieve target levels than rATG-treated patients. No significant differences in rejection rates, patient/graft survival, or rate of adverse effects were observed through 1 year.
    MeSH term(s) Adult ; Animals ; Antilymphocyte Serum/administration & dosage ; Dose-Response Relationship, Drug ; Drug Interactions ; Female ; Glucocorticoids/administration & dosage ; Graft Survival/drug effects ; Humans ; Immunosuppressive Agents/administration & dosage ; Immunosuppressive Agents/adverse effects ; Immunosuppressive Agents/pharmacokinetics ; Kidney Transplantation ; Male ; Middle Aged ; Rabbits ; Randomized Controlled Trials as Topic ; Receptors, Interleukin-2/antagonists & inhibitors ; Retrospective Studies ; Survival Rate ; Tacrolimus/administration & dosage ; Tacrolimus/adverse effects ; Tacrolimus/pharmacokinetics ; Time Factors
    Chemical Substances Antilymphocyte Serum ; Glucocorticoids ; Immunosuppressive Agents ; Receptors, Interleukin-2 ; Tacrolimus (WM0HAQ4WNM)
    Language English
    Publishing date 2015-04
    Publishing country United States
    Document type Comparative Study ; Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 424443-6
    ISSN 1536-3694 ; 0163-4356
    ISSN (online) 1536-3694
    ISSN 0163-4356
    DOI 10.1097/FTD.0000000000000125
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  8. Article ; Online: A 5-year summary of real-life dietary egg consumption after completion of a 4-year egg powder oral immunotherapy (eOIT) protocol.

    Kim, Edwin H / Jones, Stacie M / Burks, A Wesley / Wood, Robert A / Sicherer, Scott H / Leung, Donald Y M / Henning, Alice K / Lindblad, Robert W / Dawson, Peter / Keet, Corinne / Scurlock, Amy M / Plaut, Marshall / Sampson, Hugh A

    The Journal of allergy and clinical immunology

    2019  Volume 145, Issue 4, Page(s) 1292–1295.e1

    MeSH term(s) Administration, Oral ; Adolescent ; Allergens/immunology ; Anaphylaxis/drug therapy ; Child ; Child, Preschool ; Desensitization, Immunologic/methods ; Diet Therapy ; Egg Hypersensitivity/immunology ; Egg Hypersensitivity/therapy ; Egg Proteins/immunology ; Epinephrine/therapeutic use ; Female ; Humans ; Immune Tolerance ; Male ; Ovum ; Powders ; Treatment Outcome
    Chemical Substances Allergens ; Egg Proteins ; Powders ; Epinephrine (YKH834O4BH)
    Language English
    Publishing date 2019-12-24
    Publishing country United States
    Document type Letter ; Randomized Controlled Trial ; Research Support, N.I.H., Extramural
    ZDB-ID 121011-7
    ISSN 1097-6825 ; 1085-8725 ; 0091-6749
    ISSN (online) 1097-6825 ; 1085-8725
    ISSN 0091-6749
    DOI 10.1016/j.jaci.2019.11.045
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  9. Article ; Online: Clinical factors associated with peanut allergy in a high-risk infant cohort.

    Sicherer, Scott H / Wood, Robert A / Perry, Tamara T / Jones, Stacie M / Leung, Donald Y M / Henning, Alice K / Dawson, Peter / Burks, A Wesley / Lindblad, Robert / Sampson, Hugh A

    Allergy

    2019  Volume 74, Issue 11, Page(s) 2199–2211

    Abstract: Background: Prognostication of peanut allergy (PNA) is relevant for early interventions. We aimed to determine baseline parameters associated with the development of PNA in 3- to 15-month-olds with likely egg and/or milk allergy, and/or moderate to ... ...

    Abstract Background: Prognostication of peanut allergy (PNA) is relevant for early interventions. We aimed to determine baseline parameters associated with the development of PNA in 3- to 15-month-olds with likely egg and/or milk allergy, and/or moderate to severe atopic dermatitis (AD) and a positive egg/milk skin prick test (SPT), but no known PNA.
    Methods: The primary endpoint was PNA [confirmed/convincing diagnosis or last classified as serologic PNA (<2 years, ≥5 kUA/L, otherwise ≥14 kUA/L, peanut IgE)] among 511 participants (median follow-up, 7.3 years). Associations were explored with univariate logistic regression; factors with P < 0.15 were analyzed by stepwise multiple logistic regression, using data stratified by PNA status and randomly assigned to development and validation datasets.
    Results: 205/511 (40.1%) had PNA. Univariate factors associated with PNA (P < 0.01) included increased AD severity, larger egg and peanut SPT, greater egg, milk, peanut, Ara h1-h3 IgE, higher peanut IgG and IgG4, and increased pregnancy peanut consumption. P-values were between 0.01 and 0.05 for younger age, non-white race, lack of breastfeeding, and increased lactation peanut consumption. Using a development dataset, the multivariate model identified younger age at enrollment, greater peanut and Ara h2 IgE, and lack of breastfeeding as prognosticators. The final model predicted 79% in the development and 75% in the validation dataset (AUC = 0.83 for both). Models using stricter or less strict PNA criteria both found Ara h2 as predictive.
    Conclusions: Key factors associated with PNA in this high-risk population included lack of breastfeeding, age, and greater Ara h2 and peanut-specific IgE, which can be used to prognosticate outcomes.
    MeSH term(s) Allergens/immunology ; Arachis/immunology ; Female ; Follow-Up Studies ; Humans ; Immunoglobulin E/blood ; Immunoglobulin E/immunology ; Immunoglobulin G/blood ; Immunoglobulin G/immunology ; Infant ; Infant, Newborn ; Male ; Odds Ratio ; Peanut Hypersensitivity/diagnosis ; Peanut Hypersensitivity/immunology ; ROC Curve ; Risk Factors ; Skin Tests
    Chemical Substances Allergens ; Immunoglobulin G ; Immunoglobulin E (37341-29-0)
    Language English
    Publishing date 2019-07-15
    Publishing country Denmark
    Document type Journal Article ; Research Support, N.I.H., Extramural
    ZDB-ID 391933-x
    ISSN 1398-9995 ; 0105-4538
    ISSN (online) 1398-9995
    ISSN 0105-4538
    DOI 10.1111/all.13920
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  10. Article ; Online: Induction of sustained unresponsiveness after egg oral immunotherapy compared to baked egg therapy in children with egg allergy.

    Kim, Edwin H / Perry, Tamara T / Wood, Robert A / Leung, Donald Y M / Berin, M Cecilia / Burks, A Wesley / Cho, Christine B / Jones, Stacie M / Scurlock, Amy / Sicherer, Scott H / Henning, Alice K / Dawson, Peter / Lindblad, Robert W / Plaut, Marshall / Sampson, Hugh A

    The Journal of allergy and clinical immunology

    2020  Volume 146, Issue 4, Page(s) 851–862.e10

    Abstract: Background: While desensitization and sustained unresponsiveness (SU) have been shown with egg oral immunotherapy (OIT), the benefits of baked egg (BE) therapy for egg allergy have not been well studied.: Objectives: This study sought to evaluate the ...

    Abstract Background: While desensitization and sustained unresponsiveness (SU) have been shown with egg oral immunotherapy (OIT), the benefits of baked egg (BE) therapy for egg allergy have not been well studied.
    Objectives: This study sought to evaluate the safety and efficacy of BE ingestion compared with egg OIT in participants allergic to unbaked egg but tolerant to BE.
    Methods: Children who are BE-tolerant but unbaked egg reactive ages 3 to 16 years were randomized to 2 years of treatment with either BE or egg OIT. Double-blind, placebo-controlled food challenges were conducted after 1 and 2 years of treatment to assess for desensitization, and after 2 years of treatment followed by 8 to 10 weeks off of treatment to assess for SU. Mechanistic studies were conducted to assess for immune modulation. A cohort of participants who are BE-reactive underwent egg OIT and identical double-blind, placebo-controlled food challenges as a comparator group.
    Results: Fifty participants (median age 7.3 years) were randomized and initiated treatment. SU was achieved in 3 of 27 participants assigned to BE (11.1%) versus 10 of 23 participants assigned to egg OIT (43.5%) (P = .009). In the BE-reactive comparator group, 7 of 39 participants (17.9%) achieved SU. More participants who are BE-tolerant withdrew from BE versus from egg OIT (29.6% vs 13%). Dosing symptom frequency in participants who are BE-tolerant was similar with BE and egg OIT, but more frequent in participants who are BE-reactive. Egg white-specific IgE, skin testing, and basophil activation decreased similarly after BE and egg OIT.
    Conclusions: Among children allergic to unbaked egg but tolerant to BE, those treated with egg OIT were significantly more likely to achieve SU than were children ingesting BE.
    MeSH term(s) Administration, Oral ; Adolescent ; Allergens/immunology ; Child ; Child, Preschool ; Cooking ; Desensitization, Immunologic/methods ; Egg Hypersensitivity/immunology ; Egg Hypersensitivity/therapy ; Female ; Follow-Up Studies ; Humans ; Male ; Prognosis ; Treatment Failure ; Treatment Outcome
    Chemical Substances Allergens
    Language English
    Publishing date 2020-06-12
    Publishing country United States
    Document type Journal Article ; Multicenter Study ; Randomized Controlled Trial ; Research Support, N.I.H., Extramural
    ZDB-ID 121011-7
    ISSN 1097-6825 ; 1085-8725 ; 0091-6749
    ISSN (online) 1097-6825 ; 1085-8725
    ISSN 0091-6749
    DOI 10.1016/j.jaci.2020.05.040
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