Congenital HIV and Childhood AIDS

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PatientPlus articles are written by UK doctors and are based on research evidence, UK and European Guidelines. They are designed for health professionals to use, so you may find the language more technical than the condition leaflets.

See also separate article Management of HIV in Pregnancy.

HIV infection in young children most commonly arises as a result of mother-to-child transmission (MTCT). It is thought that only 1.5-2% of MTCT occurs transplacentally during pregnancy. The vast majority occurs due to maternofetal transmission of blood during parturition or postnatal breast-feeding. A negative maternal HIV test at booking does not preclude neonatal infection - maternal infection and seroconversion can occur at any time during pregnancy and lactation. This is well documented in countries with a high prevalence of HIV and has been seen in the UK.[1] 

Other routes of infection, such as precocious intravenous drug use or sexual abuse/activity, should be borne in mind as rarer scenarios, which become increasingly common as children approach adolescence.

Children suffer not only from the direct effects of AIDS itself but from the fact that their primary caregivers are very likely also to be affected or to have died from the disease. In 2014, approximately 17.8 million children had been orphaned by HIV.[2] 

The World Health Organization (WHO) estimates that in 2014 there were approximately 3.2 million cases of childhood HIV infection worldwide.[3] 

  • 91% of the world's HIV-positive children live in sub-Saharan Africa.[4] 
  • In the UK, the unlinked anonymous surveillance programme of 2011 revealed that 2.2 in 1,000 women giving birth in England and Scotland were HIV-positive.[5] 
  • In 2013, 1 in 6 HIV-positive women had not been diagnosed at the time of delivery.[6] 
  • The prevalence of UK-born women living with HIV had increased from approximately 17,000 in 2006 to 26,000 in 2013.[7] 
  • Without intervention, between 15-45% of babies born to HIV-infected mothers in the most severely affected countries are also infected.[8] With appropriate interventions transmission rates can be reduced to less than 1%.
  • Worldwide, there was a 58% reduction in the number of new HIV infections in children between 2002 and 2013. Nevertheless, more than 240,000 children were infected with HIV during 2013 - 700 new infections every day. The majority of these were infected via MTCT, during pregnancy, labour, delivery or breast-feeding.[9] 
  • By the end of March 2014, 1,873 HIV-infected children had been reported to the Collaborative HIV Paediatric Study (CHIPS - a multi-centre cohort study of HIV-infected children in the UK and Ireland). 44% were born in the UK or Ireland, 55% were born abroad and 2% were of unknown origin.[10] 

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Risk factors

The following factors increase the risk of MTCT:

  • Higher levels of maternal viraemia.
  • HIV core antigens.
  • Lower maternal CD4 count.
  • Primary HIV infection occurring during pregnancy.
  • Chorioamnionitis.
  • Co-existing other sexually transmitted infection (STI).
  • Invasive intrapartum procedures - eg, fetal scalp electrodes, forceps, ventouse.
  • Rupture of membranes (especially if delivery is more than four hours after the membranes ruptured).
  • Vaginal delivery.
  • Advanced maternal age.
  • The firstborn of twins (born to an HIV-infected mother).
  • Preterm birth.
  • Female babies more likely to be infected early (transplacental/perinatal routes).[11]
  • Co-existent malaria may increase HIV transmission rates although this is not firmly established.[12] 

It is to be hoped that most cases of UK-based HIV infection in pregnant mothers will be identified before delivery, so that HIV infection of the child is unlikely/anticipated. However, appropriate vigilance and suspicion of HIV infection in unwell children are important.

Impairment of cellular immune defences (the type found in HIV infection) should be suspected in children who present with:

  • Recurrent bacterial infections, particularly invasive infections like meningitis, septicaemia and pneumonia.
  • Recurrent/frequent common childhood infections such as otitis media, chest infection, urinary tract infections, sinusitis.
  • Unusual infections such as Mycobacterium avium complex (MAC), Pneumocystis jirovecii pneumonia.
  • Persistent oral candidiasis that fails to respond to standard therapy.
  • Recurrent or severe viral infections - eg, herpes simplex, herpes varicella-zoster infection as shingles, cytomegalovirus (CMV) retinitis.
  • Growth failure, failure to thrive or generalised wasting with no obvious nutritional, metabolic, endocrine or other cause.
  • Developmental delay, particularly language impairment, may suggest HIV encephalopathy.
  • Developmental regression caused by HIV encephalopathy or opportunistic central nervous system (CNS) infection - eg, Toxoplasma gondii.
  • Older children may show subtle diminution in intellectual skills such as concentration and memory, or schooling problems, due to HIV encephalopathy.
  • Unusual rashes: erythematous, papular rash due to HIV dermatitis, shingles rash, candidal dermatitis with marked erythema, purpura/bruising in rare cases of HIV-induced thrombocytopenia.
  • Parotid enlargement, large tonsils, oral aphthous ulcers, oral/pharyngeal plaques due to thrush or leukoplakia, CMV retinitis.
  • Signs of congestive cardiac failure due to cardiomyopathy. Peripheral oedema can also be caused by hypoalbuminaemia due to HIV nephropathy or malnutrition due to gastrointestinal dysfunction.
  • Hepatomegaly and splenomegaly are relatively common findings in HIV-infected children.

Expectant mothers should be offered routine screening for HIV infection during pregnancy. Those with positive results should be referred to a centre with expertise in managing the mother's HIV diagnosis and the pregnancy, in order to reduce the likelihood of MTCT.

Testing a child for HIV has large implications for the family, as most cases involve vertical transmission. Information given should be culturally appropriate and interpreters used as needed. See also separate article Consent to Treatment in Children (Mental Capacity and Mental Health Legislation).

Diagnostic tests

Early diagnosis of HIV infection is crucial and ideally should occur rapidly postnatally where mothers are known to be HIV-positive, as this allows for prophylaxis against and early detection of and treatment of, opportunistic infection in neonates.

Standard ELISA tests are unreliable for the first 18 months because of the transmission of maternal antibodies which persist for some time in the baby.

Polymerase chain reaction (PCR) of viral DNA can be used for early detection in infants of HIV mothers and is usually performed at 0-2 days, 6 weeks and 3 months.

Second-line, confirmatory tests include:

  • HIV RNA PCR.
  • Baseline HIV resistance (+/- maternal HIV resistance).
  • CD4 count..

Additional tests

Additional tests are performed at diagnosis to assess concurrent infection and risk of different opportunistic infection and can include:

  • Serology for hepatitis A, hepatitis B, hepatitis C, Epstein-Barr virus, CMV, herpes simplex virus, mumps, measles, rubella, VDRL and toxoplasmosis.
  • Malaria film.
  • Mantoux test/TB cultures.
  • Baseline CXR.
  • Brain ultrasound/MRI (where there are neurological signs).
  • HLAB5701 genotype (strongly associated with hypersensitivity to the antiretroviral agent abacavir). 

Monitoring

  • CD4 counts.
  • Viral load.
  • Screening - audiology, dental, neurodevelopmental, ophthalmology, TB.
  • Additional tests in line with drug therapy protocols and clinical status.

A number of clinical staging systems are available, the most common used being the Centers for Disease Control and Prevention (CDC) paediatric HIV classification and the WHO classification systems :[14][15] 

  • Category N - asymptomatic.
  • Category A - mildly symptomatic. 2 or more of:
    • Lymphadenopathy.
    • Hepatomegaly.
    • Splenomegaly.
    • Dermatitis.
    • Parotitis.
    • Recurrent/persistent upper respiratory tract infection (URTI), sinusitis or otitis media.
  • Category B - moderately symptomatic with illnesses that result from HIV infection. These include:
    • Bacterial meningitis, pneumonia or sepsis (single episode).
    • Oropharyngeal thrush lasting longer than two months.
    • Recurrent or chronic diarrhoea.
    • Lymphoid interstitial pneumonia.
    • Nephropathy.
    • Fever lasting at least one month.
    • Disseminated varicella.
  • Category C - severely symptomatic with an AIDS-defining illness.

Within these categories, a measure of immunological suppression (based on CD4 count related to age) is designated by a number (1 = no suppression, 2 = moderate suppression and 3 = severe suppression). For example, A2 refers to a mildly symptomatic child with moderate suppression of CD4 count.

In the developing world, management is largely dictated by the availability of healthcare resources and by the lack of recognition of HIV infection in pregnant women. Bottle-feeding may present significant risks in areas where there is poor access to clean, potable drinking water, and needs to be balanced against the reduction in risk of HIV transmission.

Developed world management of HIV-infected pregnant women

Antiretroviral therapy (ART) for expectant mothers and for newborns (particularly if breast-feeding).

  • ART is given to prevent MTCT and to prevent maternal disease progression. The optimal regimen is determined on a case-by-case basis according to prevailing guidelines.
  • Zidovudine (ZDV) is indicated for use in pregnancy for prevention of MTCT of HIV but single-agent ZDV therapy which does not suppress plasma viraemia to undetectable levels may allow the emergence of resistant virus.
  • Potent combinations of three or more antiretroviral drugs have now become the standard of care. (Combined ART is sometimes given the acronym cART.) Women with advanced HIV should be treated with an ART regimen. The start of treatment should be deferred, if possible, until after the first trimester and should be continued after delivery.

For further details, see separate article Management of HIV in Pregnancy.

Neonates born to HIV-infected mothers[5] 

  • ZDV monotherapy for the infant is appropriate when a mother on combination therapy delivers with a viral load of <50 HIV RNA copies/mL. Twice-daily ZDV monotherapy for four weeks is the treatment of choice.
  • Where the mother's viral load is >50 HIV RNA copies/mL, three-drug therapy should be given for four weeks. A common combination is ZDV, lamivudine and nevirapine.[16] Treatment should be started as soon as possible and no later than 72 hours after birth.
  • Babies born to untreated HIV-positive mothers should likewise receive three-drug therapy for four weeks.
  • P. jirovecii pneumonia prophylaxis, with co-trimoxazole, should be started from four weeks of age in:
    • All HIV-infected infants.
    • Infants with an initial positive HIV DNA/RNA test result until HIV has been excluded.
    • Infants whose mother's viral load at 36 weeks of gestation or at delivery is >1,000 HIV RNA copies/mL despite ART or unknown and continued until HIV infection has been excluded).

Children with confirmed HIV seroconversion

They should receive specialist paediatric infectious disease management. Children and young people should be involved as much as possible in decisions about their care, even when they are not able to make independent decisions.[17]

Antiretroviral therapy (ART)[18] 

Treatment options have improved significantly in a period of 14 years and, as for adults, the mainstay of treatment is a potent combination of antiretroviral drugs:

  • ART has significantly reduced the incidence of opportunistic infection in children and reduced mortality rates by 80-90%.[18]
  • The drugs used will vary according to the guidelines. There are current controversies in the literature with regard to triple versus quadruple therapy and the relative effectiveness, cost and toxicity of the various agents.[19] 
  • Currently, triple therapy is usual but those with a very high viral load or symptomatic disease may commence on quadruple therapy.
Important differences exist between treating children and adults for AIDS:
  • Pharmacokinetic differences: dosage is usually based on body weight and surface area but, in certain instances, a paediatric dose may exceed an adult dose - for example, with protease inhibitors, as a child's hepatic metabolism is more rapid than an adult's.
  • Dosage in children needs to be adjusted for growth.[20] 
  • Children have a relatively immature immune system.
  • CD4 counts need to be interpreted differently with different ranges according to age.
  • Natural history of AIDS is different in children compared with that of adults.
  • Potentially, children may be exposed to antiretrovirals for much longer periods of time. This is particularly important in view of the lack of long-term data regarding their safety.
  • Adherence: when to start ART critically depends on the readiness and motivation of a  child and family to embark on long-term complex medication regimes. This is usually dependent on adult caregivers and so it is important to consider supporting the family as a whole rather than the child alone. Children are frequently difficult to administer medications to and many of the drugs have previously not been available as paediatric formulations, adding to problems with compliance. Issues surrounding medication and compliance will be very different in an infant compared with an adolescent.

When should ART be started in children?

  • This is highly controversial. Whilst there are UK consensus guidelines for the use of ART in adults and neonates, similar guidelines for older children have yet to be developed. In the absence of these, European guidelines are available, published by the Paediatric European Network for Treatment of AIDS (PENTA).[20] It advocates a move away from treatment which simply prolongs survival to an approach which promotes an active and healthy life. The guidelines recommend that ART should be started:
    • In all HIV-infected children under 1 year of age.
    • In all children with significant disease (WHO stage 3 or 4 or CDC stage B or C).
    • In asymptomatic children over 1 year of age based on age-specific CD4 count thresholds (as detailed in the PENTA guidelines).
    • Before the CD4 count reaches the CD4 treatment threshold.
    • In those with hepatitis C virus or active TB co-infection.
  • Other possible indications are:
    • Asymptomatic children over 5 years at CD4 counts of 350-500 cells/μl, to potentially optimize CD4 count in adulthood.
    • Children with a high viral load (>100,000 copies/mL).
    • Asymptomatic children aged 1-3 years irrespective of immune status and viral load.
    • Sexually active adolescents, to minimise the risk of onward transmission.
    • Significant HIV-related clinical symptoms.
    • Hepatitis B virus co-infection irrespective of immune status.

The National Study of HIV in Pregnancy and Childhood, organised by CHIPS, ensures that data are available to inform management guidelines and monitor outcomes in the UK.[19] 

Prophylaxis of opportunistic infection[21] 

Standardly, HIV-positive infants receive co-trimoxazole for the first year of life (regardless of CD4 count) against P. jirovecii pneumonia. Thereafter, its continued use depends on age-specific CD4 count.

Prophylaxis for other infections is also sometimes used, either to prevent primary infection or to avoid recurrence. See current guidelines.

Immunisation

  • Routine schedule but avoid live immunisations (except measles, mumps and rubella (MMR), which is only contra-indicated in severe immunosuppression as defined by age-appropriate CD4 count).
  • Children with AIDS may not develop protective immunity from immunisation so seek advice if there is contact with measles/chickenpox, etc.
  • BCG is contra-indicated.
  • A hepatitis B course should be given from birth for the same indications as for the non-HIV-infected population - all children should receive as adolescents unless previously immunised or there are other clinical indications.
  • Vaccination should be delayed until six months of viral load <50 and CD4 >15%, if ART is required.
  • The use of pneumococcal vaccine (normally given after the age of 2) in HIV-infected children is recommended by the 'Green Book' although there are some concerns about its safety (eg, there is some evidence of reduced CD4 counts post-vaccination).[22] 
  • Varicella virus (VZV) vaccine can be considered (as in the USA) in VZV-seronegative children over 1 year of age. Two doses should be given at least one month apart and in the absence of severe immunosuppression. Administration of MMR at the same time as VZV is not advisable as this would make monitoring for attributable adverse events difficult. There should be at least a one-month gap between MMR and VZV immunisation.

Nutrition

  • Monitor weight and growth. Increase oral supplementation when nutritional deficits are identified.
  • Enteral supplementation is sometimes warranted.

Future therapies may well be generated by current research, which is looking into efficient inhibition of the HIV infection life cycle.[23]The addition of micronutrients such as zinc and vitamin A may be important in resource-poor countries but in developed countries their benefits are less clear.[24] 

  • P. jirovecii and toxoplasmosis are the primary infections seen in infected children, with P. jirovecii pneumonia being the principle cause of death.
  • Lymphocytic interstitial pneumonitis, a condition rarely seen in adults, may cause breathing to become increasingly difficult and require admission to hospital.
  • Serious bacterial infections are more common in infected children than in adults.
  • Severe and recurrent infection with Candida spp.
  • HIV encephalopathy.
  • Iatrogenic - related to side-effects and interactions from multiple medications.
  • Perinatal infection promotes accelerated disease progression in children compared with adults, due to relative immaturity of the immune system.
  • Children with untreated natural infection progress rapidly to disease and approximately 25% of children develop AIDS in the first year of life. In resource-poor settings, mortality is greater than 50% by 2 years of age.[25] 
  • Orphan status does not affect the outcome of ART providing extended family support is available.[26] 
  • Prevention of perinatal transmission necessitating appropriate medical and obstetric care through pregnancy and delivery worldwide. The widespread availability of antiretrovirals is an important aspect in the prevention of MTCT. Extended use of antiretrovirals in the postnatal period helps to prevent transmission associated with breast-feeding.
  • Education of HIV-positive children and adolescents - as HIV-infected children survive into young adulthood, they need to be aware of how to manage their developing sexual identity in light of their HIV status.
  • Consider broader responsibilities to all children in terms of HIV prevention. Health professionals may provide STI advice and treatment, without parental knowledge or consent, to those under 16 years where:[17]
    • The child understands the advice and its implications.
    • The child cannot be persuaded to tell their parents or to allow you to tell them.
    • The child is very likely to have sex without advice or treatment.
    • The child's physical or mental health will suffer without advice or treatment.
    • It is in the child's best interests.
  • Vaccine development remains an important goal.[28] 

Further reading & references

  • Tudor Car L, Brusamento S, Elmoniry H, et al; The uptake of integrated perinatal prevention of mother-to-child HIV transmission programs in low- and middle-income countries: a systematic review. PLoS One. 2013;8(3):e56550. doi: 10.1371/journal.pone.0056550. Epub 2013 Mar 6.
  • Becquet R, Marston M, Dabis F, et al; Children who acquire HIV infection perinatally are at higher risk of early death than those acquiring infection through breastmilk: a meta-analysis. PLoS One. 2012;7(2):e28510. doi: 10.1371/journal.pone.0028510. Epub 2012 Feb 23.
  1. Johnson LF, Stinson K, Newell ML, et al; The contribution of maternal HIV seroconversion during late pregnancy and breastfeeding to mother-to-child transmission of HIV. J Acquir Immune Defic Syndr. 2012 Apr 1;59(4):417-25. doi: 10.1097/QAI.0b013e3182432f27.
  2. Children Orphaned by HIV and AIDS; AVERT, 2014
  3. HIV/AIDS Fact sheet N°360; World Health Organization, 2014
  4. Statistics: Worldwide; Foundation for AIDS Research, 2014
  5. Guidelines for the management of HIV infection in pregnant women (2014 interim review); British HIV Association
  6. HIV in the United Kingdom: 2014 Report; Public Health England
  7. HIV in the United Kingdom; Public Health England, 2014
  8. Wide political support for eliminating 90 per cent of new HIV infections in children is yielding impressive results; UNICEF, 2015
  9. Children, HIV and AIDS; AVERT, 2014
  10. Summary data to the end of March 2014; Collaborative HIV Paediatric Study
  11. Biggar RJ, Taha TE, Hoover DR, et al; Higher in utero and perinatal HIV infection risk in girls than boys. J Acquir Immune Defic Syndr. 2006 Apr 1;41(4):509-13.
  12. Uneke CJ; Impact of placental Plasmodium falciparum malaria on pregnancy and perinatal outcome in sub-Saharan Africa: II: effects of placental malaria on perinatal outcome; malaria and HIV. Yale J Biol Med. 2007 Sep;80(3):95-103.
  13. HIV testing guidelines for children of HIV positive parents and/or siblings in the UK and Ireland; Children's HIV Association (CHIVA), January 2014
  14. Decle P; Treating opportunistic infections in HIV-infected children, Children's HIV Association, 2011
  15. Staging of HIV disease; aidsmap.com, 2015
  16. Mother-to-baby transmission; aidsmap.com, 2015
  17. 0-18 years guidance: Other sources of information and guidance; General Medical Council (various dates)
  18. Guidelines for the Use of Antiretroviral Agents in Pediatric HIV Infection; AIDSinfo
  19. Duong T, Judd A, Collins IJ, et al; Long-term virological outcome in children on antiretroviral therapy in the UK and Ireland. AIDS. 2014 Oct 23;28(16):2395-405.
  20. Bamford A, Turkova A, Lyall H, et al; Paediatric European Network for Treatment of AIDS (PENTA) guidelines for treatment of paediatric HIV-1 infection 2015: optimizing health in preparation for adult life. HIV Med. 2015 Feb 3. doi: 10.1111/hiv.12217.
  21. Decle P; Treatment Guidelines by OI: Fungi Pneumocystis jirovecii (formerly carinii) Pneumonia (PCP), Children's HIV Association, 2011
  22. Nunes MC, Madhi SA; Safety, immunogenicity and efficacy of pneumococcal conjugate vaccine in HIV-infected individuals. Hum Vaccin Immunother. 2012 Feb;8(2):161-73. doi: 10.4161/hv.18432. Epub 2012 Feb 1.
  23. Wang Q, Pang S; An intercellular adhesion molecule-3 (ICAM-3) -grabbing nonintegrin (DC-SIGN) efficiently blocks HIV viral budding. FASEB J. 2008 Apr;22(4):1055-64. Epub 2007 Oct 25.
  24. HIV and Nutrition; AVERT, 2014
  25. Prendergast A, Tudor-Williams G, Jeena P, et al; International perspectives, progress, and future challenges of paediatric HIV infection. Lancet. 2007 Jul 7;370(9581):68-80.
  26. Bhattacharya M, Saxena R; Outcome of anti-retroviral treatment in HIV-infected orphans and non-orphans at an ART centre in North India. Paediatr Int Child Health. 2012;32(4):228-32. doi: 10.1179/2046905512Y.0000000035.
  27. A progress report on the Global Plan towards the elimination of new HIV infections among children by 2015 and keeping their mothers alive; UNAIDS, 2012
  28. Girard MP, Picot V, Longuet C, et al; Report of the 2014 Cent Gardes HIV Vaccine Conference - Part 1: Neutralizing Antibodies; Fondation Merieux Conference Center, Veyrier du Lac, France, 5-7 October 2014. Vaccine. 2015 Mar 10. pii: S0264-410X(15)00290-X. doi: 10.1016/j.vaccine.2015.03.004.

Disclaimer: This article is for information only and should not be used for the diagnosis or treatment of medical conditions. EMIS has used all reasonable care in compiling the information but make no warranty as to its accuracy. Consult a doctor or other health care professional for diagnosis and treatment of medical conditions. For details see our conditions.

Original Author:
Dr Laurence Knott
Current Version:
Peer Reviewer:
Dr John Cox
Document ID:
1275 (v27)
Last Checked:
04/04/2015
Next Review:
02/04/2020