LIMMUNOTERAPIA AIT ATTUALE Giovanni Passalacqua Allergy Respiratory Diseases

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L’IMMUNOTERAPIA (AIT) ATTUALE Giovanni Passalacqua Allergy & Respiratory Diseases Dept. Internal Medicine. University of

L’IMMUNOTERAPIA (AIT) ATTUALE Giovanni Passalacqua Allergy & Respiratory Diseases Dept. Internal Medicine. University of Genoa ITALY

IMMUNOTERAPIA SPECIFICA (ITS) Somministrazione di estratti allergenici purificati (prima a dosi crescenti e poi

IMMUNOTERAPIA SPECIFICA (ITS) Somministrazione di estratti allergenici purificati (prima a dosi crescenti e poi a dose di mantenimento), al fine di ottenere la riduzione della risposta clinica all’allergene stesso. L’immunoterapia allergene specifica è un vaccino a tutti gli effetti La via tradizionale di somministrazione è quella iniettiva sottocutanea (SCIT), ad oggi affiancata anche dalla via sublinguale (SLIT)

Immunol Allergy Clin North Am. 2016

Immunol Allergy Clin North Am. 2016

Rands DA. Anaphylactic reaction to desensitization for allergic rhinitis and astma Br Med J

Rands DA. Anaphylactic reaction to desensitization for allergic rhinitis and astma Br Med J 1980; 281: 854 Frankland AW. Anaphylactic reaction to desensitization. Br Med J 1980; 281: 1429 Ewan PW. Anaphylactic reaction to desensitization. Br Med J 1980; 281: 1069

Committee on the safety of medicines (CMS) CMS Update Desensitizing vaccines Br Med J

Committee on the safety of medicines (CMS) CMS Update Desensitizing vaccines Br Med J 1986; 293: 948 26 fatalities since 1957 certainly due to IT 11 of them since 1980

Dal 1910 fino agli anni ’ 70: Prescrizione ingiustificata dell’ITS Prescrizione non corretta Pratica

Dal 1910 fino agli anni ’ 70: Prescrizione ingiustificata dell’ITS Prescrizione non corretta Pratica non adeguata, senza regole precauzionali e con estratti scadenti DUBBIA EFFICACIA E SCARSA SICUREZZA

Desensitizing vaccines 26 deaths due to SCIT Committee on the Safety of Medicines BMJ

Desensitizing vaccines 26 deaths due to SCIT Committee on the Safety of Medicines BMJ 1986 Non-injection routes for immunotherapy. . . the overall aim of improving safety of immunotherapy and making it more convenient for the patients. . . EAACI IT Position Paper 1993

WHO Pos Pap. Therapeutical vaccines for allergic diseases Allergy 1998 Standards for practical allergen-specific

WHO Pos Pap. Therapeutical vaccines for allergic diseases Allergy 1998 Standards for practical allergen-specific immunotherapy. Allergy 2006 Allergen immunotherapy: A practice parameter third update JACI 2011

L'ITS e' mirata all'allergene causale e non all'organo principalmente coinvolto. ” L’ITS non è

L'ITS e' mirata all'allergene causale e non all'organo principalmente coinvolto. ” L’ITS non è un trattamento di ultima scelta da usare se i farmaci falliscono, ma è complementare ad essi. L’ITS è efficace nelle allergie da - Inalanti (acari, pollini, alcuni funghi, epitelio di gatto) - Veleno di imenotteri

RINITE SINTOMI SCIT - Meta-analysis: Symptom score RINITE FARMACI Calderon M et al 2007

RINITE SINTOMI SCIT - Meta-analysis: Symptom score RINITE FARMACI Calderon M et al 2007

SYMPTOM SCORE Cochrane 2010

SYMPTOM SCORE Cochrane 2010

Meta-analysis of the efficacy of sublingual immunotherapy in allergic asthma in pediatric patients, 3

Meta-analysis of the efficacy of sublingual immunotherapy in allergic asthma in pediatric patients, 3 to 18 years of age. M Penagos, G Passalacqua, E Compalati, C Baena-Cagnani, S Orozco, A Pedroza GW Canonica SYMPTOMS MEDICATIONS

WHO pos pap (1998): 4 trials ARIA pos pap (2001): 22 trials EAACI pos

WHO pos pap (1998): 4 trials ARIA pos pap (2001): 22 trials EAACI pos pap (2006): 36 trials 1 st WAO pos pap (2009): 60 trials 2 nd WAO pos pap (2013): 77 trials After 2013: 87 trials

The optimal maintenance dose has been clearly identified (by dose-ranging studies) only for SLIT

The optimal maintenance dose has been clearly identified (by dose-ranging studies) only for SLIT tablets. The efficacy has been anyway proven over a wide range of doses, and therfore the recommendation of the manufacturers should be followed. OPTIMAL DOSES (dose-finding studies) DURHAM 2006: 15 mcg Phl p 5/day DIDIER 2007: 25 mcg Group 5 /day CRETICOS 2013: 12 mcg Amb a 1/day BERGMANN 2014: 28/120 Der p 1/Der f 1/day MOSBECH 2014: 6 SQ/day (70 mcg day) NOLTE 2015: 12 DU/day (equivalent to 6 SQ/day)

ARIA Update on immunotherapy SR Durham and G. Passalacqua JACI 2007 SCIT SLIT Clinical

ARIA Update on immunotherapy SR Durham and G. Passalacqua JACI 2007 SCIT SLIT Clinical efficacy: Rhinitis Ia Ia Clinical Efficacy: Asthma Ia Ia Clinical efficacy: Children (rhinitis) Children (asthma) Ib Ib Ia Ia Prevention of new sensitizations Ib IIa Longterm effect Ib IIa Prevention of asthma IIb

Indications Not costeffective? Mild intermitt. Mild Moderate- persistent severe intermitt. Moderatesevere persistent RHINITIS IMMUNOTHERAPY.

Indications Not costeffective? Mild intermitt. Mild Moderate- persistent severe intermitt. Moderatesevere persistent RHINITIS IMMUNOTHERAPY. ASTHMA Intermitt. HIGH RISK? Mild Moderate Severe

I fattori da valutare nella prescrizione dell’ITS 1 2 3 4 5 6 7

I fattori da valutare nella prescrizione dell’ITS 1 2 3 4 5 6 7 Il disturbo deve essere Ig. E - mediato (skin test o RAST positivi) L’allergene responsabile deve essere individuato con sicurezza Valutare la gravità e la durata dei sintomi l trattamento farmacologico é sufficientemente ben tollerato? Il paziente é in grado di affrontare l’ITS? (costi, impegno, stile di vita) È disponibile un vaccino standardizzato? L’efficacia del vaccino che si intende usare é dimostrata?

CAUSAL ROLE OF THE ALLERGEN(S): Clinical history and exposure SKIN TESTING RAST ASSAY NASAL

CAUSAL ROLE OF THE ALLERGEN(S): Clinical history and exposure SKIN TESTING RAST ASSAY NASAL (CONJUNCTIVAL) CHALLENGE MOLECULAR DIAGNOSIS SLIT (IT in general) for the clinically relevant allergen(s) Preferably one, but in selected cases 2 or 3 extracts.

BIRCH CYPRESS OLIVE 300 270 240 GRASS 210 180 150 120 90 60 30

BIRCH CYPRESS OLIVE 300 270 240 GRASS 210 180 150 120 90 60 30 jan feb mar apr may jun jul

300 MITE 270 240 210 PARIETARIA 180 150 120 GRASS 90 60 RAGWEED 30

300 MITE 270 240 210 PARIETARIA 180 150 120 GRASS 90 60 RAGWEED 30 mar apr may jun jul aug sep oct

GRASS Phl p 1 Phl p 5 Phl p 6 BIRCH Bet v 1

GRASS Phl p 1 Phl p 5 Phl p 6 BIRCH Bet v 1 PARIETARIA Par j 1 Par j 2 Phl p 7 (profilin) Phl p 12 (CBP) Bet v 2 (profilin) Bet v 3 (CBP) Par j 3 (profilin)

FATALITIES Lockey RF et al. JACI 1987 Period: 1945 -1984 46 fatalities Reid MJ

FATALITIES Lockey RF et al. JACI 1987 Period: 1945 -1984 46 fatalities Reid MJ et al. JACI 1993 Period 1985 -1989 17 fatalities FATALITIES: 1/2. 000 injections

RISK FACTORS Based on nonfatal reactions Uncontrolled asthma Severe asthma Use of betablockers Rush

RISK FACTORS Based on nonfatal reactions Uncontrolled asthma Severe asthma Use of betablockers Rush immunotherapy Use of new vials Technical errors Based on fatal reactions Uncontrolled asthma Severe asthma Use of betablockers Rush immunotherapy Build-up phase Use of new vials Technical errors Estimated incidence of fatalities < 1/2. 000 injections

SLIT No fatal event reported since 1986 15 cases of anaphylaxis in 20 years

SLIT No fatal event reported since 1986 15 cases of anaphylaxis in 20 years

SLIT: KNOWN SIDE EFFECTS Local: oral itching-swelling stomach-ache nausea-vomiting Systemic: Urticaria/angioedema Rhinitis Asthma Anaphylaxis

SLIT: KNOWN SIDE EFFECTS Local: oral itching-swelling stomach-ache nausea-vomiting Systemic: Urticaria/angioedema Rhinitis Asthma Anaphylaxis Relatively frequent. Usually self-resolve after the first doses without treatment. If persist reduce the dose. Rare. Give symptomatic treatment and reduce the dose. If persist, stop SLIT Exceptional. Treat properly and stop SLIT

Aspetti pratici. In Italia è formalmente un “named patient product” (preparato dalla ditta per

Aspetti pratici. In Italia è formalmente un “named patient product” (preparato dalla ditta per ciascun paziente dietro indicazione), anche se ad oggi i vaccini per AIT vengono preparati su scala industriale, come i farmaci e quindi uguali per tutti i pazienti. Due soli prodotti SLIT (graminacee) sono registrati come farmaco Gli estratti sono standardizzati (ossia è nota la quantità di allergene maggiore e la potenza) Con la SCIT Si effettua una fase di induzione graduale (solitamente 1/sett per 2 mesi), seguita da una fase di mantenimento (1/mese). Con la SLIT la fase di induzione può essere omessa Per allergeni pollinici si può effettuare un trattamento precostagionale. Per allergeni perenni, il trattamento è continuativo. Durata consigliata 3 -5 anni, da sospendere se dopo 2 anni non si ha beneficio.

SCIT: PRACTICAL ASPECTS • Ascertain that the dose and preparation are correct • Assess

SCIT: PRACTICAL ASPECTS • Ascertain that the dose and preparation are correct • Assess the clinical condition of the patient • Record date, hour, dose, reactions at previous injection • Use upper outer surface of arm • Ensure sterile technique • Use 1 m. L syringe • Inject at 45º by deep subcutaneous route • Record any local/systemic reaction • A waiting period of 30 min after injection is recommended

COSA OCCORRE PER LA SCIT: Adrenalina (iniezione i. m. ) Broncodilatatore short acting Steroide

COSA OCCORRE PER LA SCIT: Adrenalina (iniezione i. m. ) Broncodilatatore short acting Steroide orale e i. v. Antistaminico orale e i. v. Set da infusione Ossigeno Ambu

INDUZIONE O BUILD-UP Flac 1 0. 2 0. 4 0. 6 Flac 2 Flac

INDUZIONE O BUILD-UP Flac 1 0. 2 0. 4 0. 6 Flac 2 Flac 3 0. 2 0. 4 0. 6 MANTENIMENTO 0. 8 1 2 3 4 5 6 7 8 9 10 11 12 settimane 4 5 6 7 8 9 10 11 12 mesi

SLIT: PRACTICAL ASPECTS SLIT is self-administered at home by the patient. SLIT can be

SLIT: PRACTICAL ASPECTS SLIT is self-administered at home by the patient. SLIT can be adminstered as mono-dose vials, drops, pre dosed spray or tablets After prescription, the first dose must be given under direct medical control The preparation (drops, tablets, spray-dose) should be assumed in the morning, being the patient fastened. The dose should be kept under the tongue for 1 -2 minutes (until dissolved for tablets), then swallowed. The patient must be instructed on the possible (local) side effects, and on how to manage them.

The omission of the build-up phase seems not to increase the risk of adverse

The omission of the build-up phase seems not to increase the risk of adverse events. Build up is usually not done with the more recent tablet preparations Short build-up courses (1 -5 days) can be applied, according to the manufacturer’s suggestion and to own experience

Explain to patients the possible side effects Explain that side effects tend to disappear

Explain to patients the possible side effects Explain that side effects tend to disappear after few doses Suggest medications (e. g. oral antihistamines) to control local side effects if any Administer the first dose under medical supervision

Practical aspects. SCIT BUILD-UP: Usually recommended (4 -8 wks) MAINTENANCE: usually every 4 wks

Practical aspects. SCIT BUILD-UP: Usually recommended (4 -8 wks) MAINTENANCE: usually every 4 wks DURATION: 3 -5 yrs PROTOCOL: continuous or pre-coseasonal (with the MPLadjuvanted SCIT, only 4 preseasonal injections) SLIT PREPARATION: drops, pre-dosed spray, tablets BUILD-UP: Very short (days) or absent MAINTEINANCE: Preferably daily (can vary according to the manufacturer). DURATION: 3 -5 yrs PROTOCOL: Preferred pre- coseasonal (continuous for HDM)

INIZIO: Prima della stagione di pollinazione (2 mesi) In qualsiasi momento per i perenni

INIZIO: Prima della stagione di pollinazione (2 mesi) In qualsiasi momento per i perenni SCHEMA: Tradizionale, cluster, rush MANTENIMENTO: Prestagionale, precostagionale, continuo DURATA: Almeno 3 -5 anni, poi se beneficio sospendere Se non beneficio dopo 2 anni sospendere VALUTAZIONE: Clinica (riduzione dei sintomi e dei farmaci)

PREMEDICATION: PROS: Preventing reactions Avoiding severe reactions Diminishing reactions’intensity ? CONS: May mask symptoms’

PREMEDICATION: PROS: Preventing reactions Avoiding severe reactions Diminishing reactions’intensity ? CONS: May mask symptoms’ onset May delay appropriate treatment

JACI 2016

JACI 2016

EFFETTI “SPECIALI” DELL’AIT Efficacia a lungo termine dopo la sospensione Prevenzione di nuove sensibilizzazioni

EFFETTI “SPECIALI” DELL’AIT Efficacia a lungo termine dopo la sospensione Prevenzione di nuove sensibilizzazioni Riduzione del rischio di insorgenza di asma Modificazione della risposta immunitaria

AIT: carry-over EFFECT Passalacqua G. Ann Allergy Asthma Immunol. 2011; 107: 401– 406.

AIT: carry-over EFFECT Passalacqua G. Ann Allergy Asthma Immunol. 2011; 107: 401– 406.

AUTHOR (ref) ALLERGEN Mosbech (36) Grass Grammer (37) Ragweed Hedlin (38) PATIENTS DURATION SIT

AUTHOR (ref) ALLERGEN Mosbech (36) Grass Grammer (37) Ragweed Hedlin (38) PATIENTS DURATION SIT LONG-LASTING EFFECT 2. 5 years 61 adult/children 4 months 2 years Cat/dog 32 adult/chidren 3 years 5 years Des Roches (39) Mite 40 adult 1 -4 years 3 years Ariano (40) Parietaria 35 adult 4 years Durham (41) Grass 52 adult 3 -4 years 3 years Eng (43) Grass 25 children 3 years 12 years

Specific immunotherapy has long -term preventive effect of seasonal and perennial asthma: 10 -year

Specific immunotherapy has long -term preventive effect of seasonal and perennial asthma: 10 -year follow-up on the PAT study Jacobssen, Allergy 2007

PREVENTIVE EFFECTS OF SUBLINGUAL IMMUNOTHERAPY IN CHILDHOOD. AN OPEN RANDOMIZED CONTROLLED STUDY MAURIZIO MAROGNA

PREVENTIVE EFFECTS OF SUBLINGUAL IMMUNOTHERAPY IN CHILDHOOD. AN OPEN RANDOMIZED CONTROLLED STUDY MAURIZIO MAROGNA MD 1 , D. TOMASSETTI 1, A. BERNASCONI 1, F. COLOMBO 1, ALESSANDRO MASSOLO BS 2, A. DI RIENZO BUSINCO 4, GIORGIO W CANONICA MD 3, GIOVANNI PASSALACQUA MD 3 AND SALVATORE TRIPODI MD 4 1 3 Pneumology Unit, Cuasso al Monte, Macchi Hospital Foundation, Varese 2 Department of Animal Biology, University of Pavia, Pavia Allergy & Respiratory Diseases, Department of Internal Medicine, Genoa University 4 Pediatric Allergy Unit, S. Pertini Hospital, Rome AAAI 2008, 101: 261

MONOSENSITIZED PATIENTS 70 70 60 60 *** 50 40 % PATIENTS PERSISTENT ASTHMA ***

MONOSENSITIZED PATIENTS 70 70 60 60 *** 50 40 % PATIENTS PERSISTENT ASTHMA *** 30 *** 50 40 30 20 20 NS 10 10 baseline CONTROLS 3 rd year baseline 3 rd year SLIT

New approaches for Immunotherapy ADMINISTRATION RECOMBINANT/ ENGINEERED Milk Egg Peanut Food allergy NEW INDICATIONS

New approaches for Immunotherapy ADMINISTRATION RECOMBINANT/ ENGINEERED Milk Egg Peanut Food allergy NEW INDICATIONS Latex Atopic dermatitis Nickel? Liposomes Intralymphatic (ILIT) Epicutaneous (EPIT) Biolistic injection Mucoadhesive substances Alum-alginates ADJUVANTS Bacterial wall derived DNA-adjuvants Recombinant purified Hypoallergenic isoforms Peptides Chimeric proteins (constructs) c-DNA GENIC VACCINATION Plasmids Replicons

Passalacqua G, Canonica GW. WAO J 2015

Passalacqua G, Canonica GW. WAO J 2015

FARMACI Azione rapida Effetto preventivo NO SI Effetti collaterali SI Costo BASSO Lunga durata

FARMACI Azione rapida Effetto preventivo NO SI Effetti collaterali SI Costo BASSO Lunga durata SIT NO NO ALTO SI

CONCLUSIONI Farmacoterapia e immunoterapia hanno meccanismi diversi Il loro effetto è additivo L’ITS consente

CONCLUSIONI Farmacoterapia e immunoterapia hanno meccanismi diversi Il loro effetto è additivo L’ITS consente un risparmio di farmaci sintomatici L’ITS ha effetti preventivi e a lungo termine che i farmaci non hanno L’ITS agisce contemporaneamente su naso e bronchi FARMACI E ITS NON SONO MUTUAMENTE ESCLUSIVI