IPV in Moderate to Severe Chronic Malnourished 9-12 Month Old Children in Karachi. (MIPV)

Aga Khan University

Status and phase: Completed; Phase 4

Conditions: Immunity to Polio Vaccines in Non-malnourished Infants; Immunity to Polio Vaccines in Malnourished Infants

Treatments: Biological: Injectable polio vaccine and Bivalent oral polio vaccine

Study type: Interventional

Funder types: Other; NIH

Identifiers

NCT01695798

MIPV

ACTRN 12612000259842 (Registry Identifier)

Details and patient eligibility

About

Chronic malnutrition is associated with lack of effective gut immunity which is a possible explanation for why we see polio cases among a proportion of children who have received 7 or more doses of OPV.Our proposed idea is to evaluate if IPV antigen given later in life may act together to boost humoral and mucosal immunity in children belonging to low-income background in Karachi who have moderate to severe chronic malnutrition (height for age Z score less than -2SD). We also intend to compare eIPV + OPV with OPV only in non-malnourished infants at 9 -12 month of age. Thus, the proposed study is a combination of two trials, with study population stratified by nutritional status, each with a reference arm (bOPV) and an experimental arm (bOPV plus IPV).

Full description

The development of chronic malnutrition is a complex interplay of multiple factors; including genetic predisposition and a whole host of environmental insults. In the urban squatter and peri-urban settlement environments of Karachi where the Aga Khan University (AKU) has established surveillance programs, half of all infants have moderate to severe chronic malnutrition (height for age Z score less than -2 SD) by the time they are 9 -12 months old. IPV has the advantage of parenteral route, thereby bypassing the damaged gut mucosa of malnourished children. It also does not cause the rare vaccine-associated paralysis. Its effectiveness depends on stimulation of serum (blood) neutralizing antibodies that block the spread of poliovirus to the central nervous system. The main disadvantages that have precluded IPV use in low-income countries is high cost, difficulty in adding another injectable vaccine in the EPI schedule at 6, 10, and 14 weeks, and lack of ability to induce a strong mucosal immune response and therefore prevent enteral infection. Additionally, maternal antibodies at this early age neutralize IPV quite effectively. However, as the median age of polio in Pakistan is 15 months for poliovirus type 1 and 18 months for poliovirus type 3, it may be feasible to give a single IPV dose at an older age, avoiding the effects of maternal antibodies and boosting immunity against polio before the majority of these children enter their risk period in Pakistan. Enhanced potency IPV (eIPV) with higher antigen content yields greater than 90% seropositivity against all 3 types after one dose and 100% seropositivity after two doses. Thus using eIPV combined with OPV at 9 - 12 months in moderate to severe chronically malnourished infants may provide improved seroconversion as well as some stimulation of the mucosal immune response. Our proposed idea is to evaluate if IPV antigen given later in life may act together to boost humoral and mucosal immunity in children belonging to low-income background in Karachi who have moderate to severe chronic malnutrition (height for age Z score less than -2SD). We also intend to compare eIPV + OPV with OPV only in non-malnourished infants at 9 -12 month of age. Thus, the proposed study is a combination of two trials, with study population stratified by nutritional status, each with a reference arm (bOPV) and an experimental arm (bOPV plus IPV).

Enrollment: 840 patients

Sex: All

Ages: 9 to 12 months old

Volunteers: Accepts Healthy Volunteers

Inclusion criteria

• Infant aged 9 - 12 months of age
• Resident of the study area for last 3 month at the time of enrolment
• Parent/guardian provides informed consent

Exclusion criteria

• Infant already enrolled in any other polio intervention study.
• Infant found acutely ill at the time of enrolment, requiring emergent medical care
• Infant with moderate and severe acute malnutrition, defined by a very low weight for height (below -2z and -3z scores of the median WHO growth standards respectively).
• Refusal of blood testing
• Receipt of supplementary dose of OPV within 4 weeks of first study visit
• Infant with certain medical conditions i.e., cerebral palsy, syndromic infants, infants on corticosteroids because of any medical illness, thrombocytopenia (contraindication of intramuscular injections), malignancies and infant with primary immunodeficiency

Trial design

Primary purpose: Prevention

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: None (Open label)

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840 participants in 4 patient groups

Chronic malnourished bOPV

No Intervention group

Description:

This arm will receive only bOPV

Malnourished IPV+bOPV

Experimental group

Description:

This arm will receive IPV and bOPV

Treatment:

Biological: Injectable polio vaccine and Bivalent oral polio vaccine

Normally nourished bOPV

No Intervention group

Description:

This arm will receive only bOPV

Normally nourished IPV+bOPV

Experimental group

Description:

This arm will receive both IPV and bOPV

Treatment:

Biological: Injectable polio vaccine and Bivalent oral polio vaccine