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Challenges in Pediatrics Taking Toddlers to Teens and Beyond. Lynne M. Mofenson, M.D . Maternal and Pediatric Infectious Disease Branch Eunice Kennedy Shriver National Institute of Child Health and Human Development National Institutes of Health. Topics to Discuss. Infants Early treatment
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Challenges in PediatricsTaking Toddlers to Teens and Beyond Lynne M. Mofenson, M.D. Maternal and Pediatric Infectious Disease Branch Eunice Kennedy Shriver National Institute of Child Health and Human Development National Institutes of Health
Topics to Discuss • Infants • Early treatment • Viral reservoir • Perinatally-infected adolescents • Complications • Transition
Importance of Early Therapy in HIV-Infected Infants • We know that early ART – in the first 3 months of life – significantly decreases morbidity and mortality. Probability of Death 75% Reduction in Mortality: 4% vs 16% for Early vs Deferred ART Probability of Death or Progression 77% Reduction in Death/ Progression: 6% vs 26% for Early vs Deferred ART
Early Treatment Restricts the Proviral Reservoir Persaud D et al. JAMA Pediatr 2014;in press Proviral Reservoir Size & Age at Virologic Control in Perinatal Youth • 144 Youth with Perinatal Infection and Suppressed Virus in PHACS • Median Age: • 14.3 Yrs • Median cART duration: • 10.2 yrs >5 yr <1 yr HIV DNA (copies/million PBMCs) Age at Virologic Control: <1 yr old 1-5 yrs old >5 yrs old
However - Sustained Elevation of Immune Activation Markers Regardless of Starting ART Age <1 Yr with Durable SuppressionPersaud D et al. JAMA Pediatr 2014;in press P-value PHIV+ vs HEU: <0.001 <0.001 0.004
However - Sustained Elevation of Immune Activation Markers Regardless of Starting ART Age <1 Yr with Durable SuppressionPersaud D et al. JAMA Pediatr 2014;in press Early ART (starting <1 year) led to smaller proviralreservoir but did not reverse immune activation (elevated in all 3 groups vs HIV-exposed uninfected controls) P-value PHIV+ vs HEU: <0.001 <0.001 0.004
Restricted Viral Reservoir with Early ART: ThailandAnanworanich J et al. AIDS 2014;28:1015-20 15 children, median 6.3 yrs, who started ART age <6 mos (median 17 wks); median duration viral suppression 6 years. • Early ART results in restricted viral reservoir • Restricted immune response: 93% had no HIV-specific CD4 or CD8 response • 47% non-reactive on EIA Median 17 copies/106 132 copies/106 None detectable 60% had <20 c/106
Latent CD4 Reservoir Dynamics in Infants Starting ART Age <6 Months - Lower Reservoir if Starting Age <6 Weeks Persaud D, et al. AIDS 2012;26:1483-90 P1030 LPV/r infant PK study: 17 infants, median age 8.1 wks at start of ART, with RNA <400 by 24 wks ART, <400 through 96 wks • Lower reservoir size in infants treated before six weeks of age • Reservoir decays during the first 2 years of life but remains detectable in most at 2 years of age • half-life of 11 months [95% CI: 6 to 30 mos] Start ART <6 wk/o Start ART >6 wk/o
Restricted Proviral Reservoir in Children Receiving Early Treatment with Sustained Viral ControlLuzuriaga K et al. J Infect Dis 2014 May 21; Epub ahead print
Proviral Reservoirs Have Continuous Decay in Children with Early Therapy Luzuriaga K et al. J Infect Dis 2014 May 21; Epub ahead print p=0.03 p=0.02 p=0.01 p=0.17 Median proviral load (IQR) in early-treated youth, by age Age at sample (yr) HIV Proviral Decay Cures Among Individual Children With Early Treatment, by Age at Sample
Early Therapy is Associated with Loss of HIV-Specific Immune Response - Western Blot Antibody Findings Luzuriaga K et al. J Infect Dis 2014 May 21; Epub ahead print Early-treated youth lose response to HIV proteins over time Late-treated youth retain strong response to all HIV proteins
Early Treatment (<1 yr, <6 mos, <6 wks) Restricts Reservoir - What About Treatment Starting at Birth? Very Early Treatment = Potential “Functional Cure”? “Viral Remission” as Opposed to “Cure”?
“The fact that this child was able to remain off antiretroviral treatment for two years and maintain quiescent virus for that length of time is unprecedented.” “The prolonged lack of viral rebound, in the absence of HIV-specific immune responses, suggests…the very early therapy not only kept this child clinically well but also restricted the number of cells harboring HIV infection.” “The case of the Mississippi child indicates early antiretroviral treatment…did not completely eliminate the reservoir….but may have considerably limited its development and averted the need for antiretroviral medication overs a considerable period”
Is Early Time-Limited ART Possible? CHER Trial Cotton M et al. Lancet 2013;382:1555-63 Immediate ART x 40 WKS Early ART to 40 weeks; then STOP, until progression N=125 HIV diagnosed before 12 wks (median 7.4 wks) & CD4% ≥25% N=375 ART-Deferred Immediate ART x 96 WKS Defer ART until clinical progression or CD4% drop Early ART to 96 weeks; then STOP, until progression N=125 N=125 ART (start or re-start) when CD4% <20% or clinical event 1st-line ART: LPV/r+ZDV+3TC Median follow-up 4.8 years Primary endpoint: time to failure of first line ART
CHER Study: Early Time-Limited ART Cotton M et al. Lancet 2013;382:1555-63 Immediate x 40 wk Immediate x 96 wk Restart ART after interruption Deferred Start ART Median time to restart ART 33 wks IQR 26-45 19% not restarted Median time to start ART 20 wks IQR 16-25 Median time to restart ART 70 wks IQR 35-109 32% not restarted
CHER Study: Early Time-Limited ART Cotton M et al. Lancet 2013;382:1555-63 • Early time-limited ART superior to deferred ART over an extended period • Deferred ART had more time on ART yet highest # deaths, clinical events, hospital admissions • Similarities with Mississippi baby? Consistent with early ART potentially restricting viral reservoir, longer duration ART before interruption
Early Treatment and “Functional Cure” • Early ART studies and Mississippi baby have shown: • Potential significant restriction (but not yet elimination) of viral reservoir with very early ART • Continuing decline in reservoir over time • Loss of HIV-specific immune responses • “Remission” of HIV off ART • Many questions remain: • How to measure the latent pool in infants? • If reservoir establishment can’t be blocked, when should eradication attempts begin? • Should immune approaches be studied to increase HIV-specific immune response? • How long can viral “remission” be prolonged?
AdolescentsProlonged SurvivalEmerging Issues Jim Oleske, UMDNJ Newark Long-term survivors, 2003
Estimated Number of Children Aged <15 Years Living with HIV in Sub-Saharan Africa 2020: 1,931,768 (1,905,934 – 1,933,598) WHO March 2014 Supplement to 2013 Guidelines
Children with Perinatal HIV Infection are Now Surviving for Prolonged Periods • HIV-infected children now aging into adolescence. • HIV has become a chronic disease with all its concomitant challenges such as adherence to therapy, psychosocial challenges, sexual activity. • Newly recognized late complications are being detected with chronic HIV infection as well as a consequence of its therapies.
Complications of HIV and Antiretroviral Therapy in Children • Metabolic complications • Abnormal fat accumulation & wasting • Abnormal lipid profiles • Insulin resistance • Osteopenia/bone disease • Mitochondrial toxicity • Liver disease • Renal disease • Cardiac disease • Mental health • Obesity
Challenges in Adolescent HIV Care • Knowledge of HIV infection (disclosure). • Linking to (and retaining in) health care. • Accepting (and adhering to) therapy. • Mental health issues. • Complexities of transition to adult care. • High risk population for HIV transmission. • 40-60% of HIV-infected adolescents may engage in unprotected sex. • High rate substance use, smoking. Kadivar H et al. AIDS Care 2006;18:544-9 Rotheram-Borus M et al. J Adoles 2001;24:791-802 Lightfoot M et al. Am J Health Behav 2005;29:162-71. Rice E et al. Prospect Sex Repro Health 2006;38:162-7 Murphy DA et al . J Adol Health 2001;29S:57-63 Sturdevant MS et al. J Adol Health 2001;29S:64-71
Perinatally-Infected Youth are Sexually ActiveTassiopoulos K et al. Clin Infect Dis 2013;56:283-990 Annual audio computer-assisted interviews (ACASI) in 377 youth >10 years with perinatal HIV infection in Pediatric HIV/AIDS Cohort Study in US. • 28% were sexually active at initial/follow-up ACASI. • 67% of 18-year olds had initiated sex. • Mean age of initiation=13 yrs for males, 14 yrs for females Age (yrs) at most recent ACASI
Challenge: Pregnancy in Perinatally-Infected Females • Between1998-2013, 16 publications on 277 pregnancies in 231 perinatally-infected girls.
Challenge: Pregnancy in Perinatally-Infected Females • Between1998-2013, 16 publications on 277 pregnancies in 231 perinatally-infected girls. • Majority of pregnancies were unplanned. • Elective termination was not uncommon (15%-42% in 5 studies reporting). • Repeat pregnancy was not uncommon: 32 had 2 pregnancies; 4 had three pregnancies. • Adverse pregnancy outcomes: miscarriage (6-14% 4 studies), preterm (7-44% 4 studies),SGA (47% 1 study), low birth weight (1 study). • MTCT uncommon (3 infections/159 live birth, 2%).
Transition to Adult Care: Mortality in Perinatally-HIV-Infected Youth In UK/IrelandFish R et al. HIV Med 2013 Sept 25 (Epub ahead print) • Evaluated mortality 2006-2011 in UK/Ireland in 996 perinatally-infected youth >13 years, including 248 cared for in14 adult clinics. Median age at transfer 17 years and at death 21 years. • Estimated minimum mortality by age and type care in perinatally HIV-infected young people UK/Ireland:
Transition to Adult Care: Mortality in Perinatally-HIV-Infected Youth In UK/IrelandFish R et al. HIV Med 2013 Sept 25 (Epub ahead print) Complex medical and psychosocial issues in perinatally infected young adults – 82% of deaths associated with poor adherence and advanced HIV disease, 9 with mental health diagnoses and 2 deaths due to suicide! • Evaluated mortality 2006-2011 in UK/Ireland in 996 perinatally-infected youth >13 years, including 248 cared for in14 adult clinics. Median age at transfer 17 years and at death 21 years. • Estimated minimum mortality by age and type care in perinatally HIV-infected young people UK/Ireland: Wednesday July 23 Living with HIV – Transitions to Adulthood 13:00-14:00 Room 105-106
Summary: From Tots to Teens • While we don’t have a “cure”, very early ART of infected neonates has promise in significantly restricting the viral reservoir and “remission”. • Potential utility of stimulating HIV-specific immune response in such children to prolong “remission”. • Even with “elimination” of pediatric HIV, millions of perinatally-infected youth will continue to survive into adolescence and young adulthood for many years to come. • We need to address new challenges with such youth, including late complications HIV/ART, sexual activity, transition to adult care.
Thanks For Your Attention