Silent casualties from the measles outbreak in South Africa.
The measles virus is highly contagious, and outbreaks are fuelled by overcrowding and poor vaccine coverage, making elimination status in South Africa difficult to attain. Measles may infect the central nervous system (CNS) as acute viral encephalitis, or result after 2-4 weeks in a post-infectious immune-mediated inflammatory disorder or acute disseminated encephalomyelitis (ADEM). There are 2 further rare and latent CNS complications resulting from a preceding measles infection: subacute sclerosing panencephalitis (SSPE) caused by years of viral persistence in a seemingly immunocompetent host, (3) and subacute measles encephalitis (SME), occurring in an immunocompromised host. (4)
SME manifests 1-7 months after the acute measles infection. (5) Patients present with seizures, often epilepsy partialis continua, and altered mental status. (5) It carries a mortality rate of 85% and survivors often have significant psychomotor retardation.5 SME has hitherto only been described in single case reports as a rare complication of measles in the context of organ transplantation,6,7 immunosuppressive therapy or immunodeficiencies, (5,8) and HIV and AIDS. (5,9,10) We report 8 cases of SME in HIV-infected patients who presented to a tertiary referral hospital between July and October 2010.
The index case (Patient 1), known to be HIV-positive, presented with a 2-week history of focal twitching and clumsiness of the right hand and secondary generalised seizures on 3 occasions. Three months earlier, she contracted measles complicated by pneumonitis (Table I). She was unable to recall ever receiving measles vaccination. She recovered and commenced antiretroviral treatment (ART) 4 weeks later as well as co-trimoxazole prophylaxis. Her nadir CD4 cell count was 67 cells/[micro]l. She had never travelled and did not abuse illicit substances.
Other than the epilepsy partialis continua (focal motor status epilepticus) of the right hand with dystonic posturing of the left foot and intermittent leg twitching, she was initially relatively well. She reported no headache, and on examination was afebrile, co-operative and not encephalopathic. Serum biochemistry including glucose was normal. She had evidence of immune reconstitution with a CD4 count of 286 and an undetectable serum HIV viral load. Cerebrospinal fluid (CSF) was acellular with normal biochemistry and negative tests for neurosyphylis and cryptococcal antigen. CSF cultures for bacteria, fungi and tuberculosis were negative. CSF polymerase chain reaction (PCR) tests were repeatedly negative for herpes simplex virus 1 and 2, cytomegalovirus, JC virus, Epstein Barr virus, herpesvirus 6, fungi, toxoplasmosis, enteroviruses and measles. The HIV viral load in the CSF was undetectable. The electroencephalogram (EEG) showed left periodic lateralised epileptiform discharges (PLEDs). Brain imaging showed no abnormalities, but there was subtle non-enhancing left frontal cortical hyperintensity on the TR sequences of the initial MRI (week 3 of SME).
The patient deteriorated rapidly over the following weeks from being independent to requiring assistance with walking and feeding. Her vision deteriorated and she developed dilated, sluggishly reactive pupils. There was no evidence of corneal or retinal involvement and no papiloedema. A repeat brain MRI showed contiguous spread of the left frontal lesion (Fig. 1) and additional multifocal T2-hyperintensities, but again limited to the cortical ribbon. A brain biopsy revealed non-necrotising encephalitis with eosinophilic inclusions, suggestive of viral aetiology. Measles PCR on brain tissue was positive, confirming SME. The seizures were finally controlled with a combination of valproate, levitiracetam and clonazepam. Despite commencement on oral ribavirin, her level of consciousness deteriorated. She is currently mute and unresponsive.
We identified a further 7 patients with either definite or probable SME. We classified as 'definite SME' a suggestive clinical picture (focal seizures and/or encephalopathy) and a positive measles PCR in either brain biopsy, CSF or urine. 'Probable SME' was diagnosed in the context of a suggestive clinical picture, normal CSF findings in the absence of other identifiable pathogens, and with supportive features such as MRI demonstrating multifocal grey matter signal abnormalities and/or positive CSF measles serology (IgG).
Table I shows the clinical characteristics of the 8 patients with definite and probable SME (N=3). The median age was 28 years (range 14-38); all were HIV-positive (newly diagnosed in 3); one was known to be on ART at the time of measles infection. The median CD4+ count at presentation was 37 (range 1-268); 4 had a history of a morbiliform rash, and the median time to presentation with SME following rash was 12.5 weeks. All patients developed seizures, but 3 presented with focal motor status or epilepsia partialis continua. Blindness and deafness constituted the other modes of presentation. Patient 2 developed hearing loss a few weeks after being immunised against measles as part of the nationwide measles campaign (his HIV status unknown at the time). Subsequent genotyping of the measles virus detected in his CSF revealed wild-type measles and not the vaccine strain. SME was fatal in 6 patients, and the mean time between onset of SME and death was 21 days. The clinical and radiological picture of patient 8, who may have been on ART at the time of measles infection, appears to have stabilised prior to the initiation of ribavirin between 9 and 10 weeks. He presently has normal higher mental functions and seizures are controlled on valproate.
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The laboratory and radiological investigations are shown in Table II. Routine CSF examinations were non-contributory. The MRI appearance was remarkably similar in trie 7 patients scanned: T2-signal abnormality in a distinctive patchy cortical distribution, but in some also involving the deep basal ganglia consistent with a polioencephalopathy. White-matter abnormalities were variable and infrequent.
This is the largest SME case series to date--and, alarmingly, collected over 4 months. All patients were HIV-positive and, with one exception, had CD4 counts <100 cells/[micro]l at the time of measles infection, consistent with SME as an opportunistic infection in an immunocompromised host. (4) The measles virus enters the CNS with the initial viraemia, but it is thought that a poor cell-mediated immune response allows virus to persist n this compartment with the potential fiar SME. (4) Interestingly, the 2 survivors were those with the least compromised CD4 counts; one had reconstituted on ART and the other was the least affected clinically. In immunosuppressed animals infected with the measles virus, the repopulation of lymphocytes was associated with the elimination of viraemia, (4) suggesting that immune reconstitution in HIV-infected patients may enable a more robust immune response. Furthermore, human leukocyte antigen (HLA) polymorphisms influence measles antibody responses, which may be a modifying factor influencing susceptibility to this measles complication. (11)
Focal seizures are well described in SME although the mechanism by which the measles virus induces epileptogenicity is not clear. When neurotropic measles virus is inoculated into mouse brain, neuroglial excitotoxicity (probably via N-methyl D-aspartate (NMDA)-receptor signaling) preceded neuronal hyperexcitability resulting in intermittent and later continuous seizures, followed by neuronal cell loss. (12)
Acute onset visual loss and deafness have been infrequently reported in SME; however, sensorineural hearing loss, (13) keratitis and corneal scarring resulting in blindness, particularly in the presence of vitamin A deficiency, are known complications of acute measles. (13) Preferential involvement of occipital, thalamic and putaminal areas occur in SSPE. (14) In our patients with visual impairment, there was clinical evidence of anterior visual pathway involvement (abnormal pupillary responses) and, on MRI, posterior (occipital and/or temporal lobe) visual pathway involvement (Fig. 2). The recognition of visual and hearing loss may be important in considering a diagnosis of SME.
SME is an elusive diagnosis. The preceding measles rash may be subtle or absent in an immunocompromised host. (4) The CSF examination may be normal, and specific measles testing using antibodies and more sensitive PCR may be negative. Absence of measles virus DNA in the CSF is probably due to the intraneuronal location of the measles virus and, unlike non-neuronal cells, viral budding and shedding does not occur in the CNS. (15) Further, in the CNS, measles viral transmission occurs via trans-synaptic neuronal spread, (15) which may explain the contiguous cortical spread on sequential MRI brain images (Figs 1a, b). Therefore, in the absence of finding evidence of ongoing measles virus infection in the CSF, a definitive diagnosis would require brain biopsy.
Two outbreaks of measles have occurred in South Africa in the last decade, with one still ongoing.16 Failure to vaccinate a critical percentage of the population is the probable cause. Vaccine effectiveness may be lowered in HIV infection, but the population vaccine effectiveness remained high,16 underscoring the importance of immunisation programmes in an HIV-endemic population.
The fatal intersection of HIV and measles has resulted in a cluster of patients in South Africa with subacute measles encephalitis, many of whom might have died before reaching medical attention, which serves to remind clinicians of the importance of a vigilant and effective measles immunisation programme. By reporting these patients who present with focal seizures, often with hearing and visual loss and with evidence of a polioencephalopathy on MRI, we aim to raise awareness of this devastating complication. Although insensitive, we propose the use of measles virus PCR in CSF and/or urine as a time- and cost-effective way of confirming the diagnosis of SME in the absence of a brain biospy.
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The authors thank the Groote Schuur Hospital doctors who referred their cases, and Drs Hewlett and Tu who assisted with the neuropathological examinations of the post mortem specimens. HvdP is funded by PEPFAR/ USAID through the ANOVA Health Institute. The UCT research ethics committee approved the reporting of the clinical material (487/2010).
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Christine Albertyn, Edward B LeePan and Jeannine M Heckmann are affiliated to the Division of Neurology, Department of Medicine, University of Cape Town; Helen van der Plas to the Division of Infectious Disease and HIV Medicine, Department of Medicine, University of Cape Town; Diana Hardie to the Division of Virology, Department of Clinical Laboratory Sciences, University of Cape Town and the National Health Laboratory Service; Sally Candy to the Department of Radiology, University of Cape Town; and Tamiwe Tomoka to the Division of Anatomical Pathology, Department of Clinical Laboratory Sciences, University of Cape Town and the National Health Laboratory Service.
Corresponding author: J Heckmann (Jeanine.Heckmann@uct.ac.za)
Table I. Characteristics of subjects at presentation of subacute measles encephalitis (SME) Pt 1 Pt 2 Pt 3 * Pt 4 Age (years) 27 14 29 25 Gender F M F M HIV status known Y N N N CD4 count (cells/[micro]l) Presentation 268 1 66 11 CD4 nadir ([dagger]) 65 - - - Measles infection History of rash + + - - History of pneumonitis + + - - On ART N N N N Period of clinical latency (weeks) 15 10 UK UK Presenting SME symptom Focal motor seizure + Hearing loss + Visual loss + Generalised motor seizure + SME symptomatology EPC/generalised seizure +/+ +/+ +/- Blindness + - - + Encephalopathy + + + + Outcome Follow-up time (weeks) 12 4 2.5 2 Death NA Y Y Y Pt 5 * Pt 6 Pt 7 * Age (years) 32 34 24 Gender F F F HIV status known Y Y Y CD4 count (cells/[micro]l) Presentation 47 26 11 CD4 nadir ([dagger]) 15 26 11 Measles infection History of rash - + + History of pneumonitis + - - On ART UK Y N Period of clinical latency (weeks) UK 3 16 Presenting SME symptom Focal motor seizure + + Hearing loss + Visual loss Generalised motor seizure + SME symptomatology EPC/generalised seizure +/- +/+ +/+ Blindness + -- - Encephalopathy + + + Outcome Follow-up time (weeks) 6 3.5 1.5 Death Y Y Y Pt 8 Age (years) 38 Gender M HIV status known Y CD4 count (cells/[micro]l) Presentation 225 CD4 nadir ([dagger]) 148 Measles infection History of rash - History of pneumonitis - On ART Y ([double dagger]) Period of clinical latency (weeks) UK Presenting SME symptom Focal motor seizure Hearing loss Visual loss + Generalised motor seizure + SME symptomatology EPC/generalised seizure -/+ Blindness + Encephalopathy - Outcome Follow-up time (weeks) 9 Death NA * Refers to probable cases, the remainder are definite cases (see text). ([dagger]) If known. ([double dagger]) Patient on ART for 1 year preceding presentation. M = male; F = female; Y = yes; N = no; ART = antiretroviral therapy; UK = unknown; EPC = epilepsy partialis continua; NA = not applicable. Table II. Laboratory, pathology and radiological investigations in subjects Pt 1 Pt 2 Pt 3 CSF Normal Normal Normal Measles antibodies Serum IgG Pos Neg Pos CSF IgG Neg Neg Pos Measles PCR Urine ND ND ND CSF Neg Pos Neg Brain biopsy Pos ND ND *, ([dagger]) EEG PLEDS PLEDS PLEDS CT brain Normal Normal Normal Location of MRI signal abnormalities Superficial grey matter + + + Deep grey matter - + + White matter - + - Histopathology INI ND INI Pt 4 Pt 5 Pt 6 CSF Normal Normal Normal Measles antibodies Serum IgG Pos Pos ND CSF IgG ND Neg ND Measles PCR Urine Pos Neg Neg CSF Pos Neg Neg Brain biopsy ND ND Pos * EEG Slowing Slowing PLEDS CT brain Normal Normal Normal Location of MRI signal abnormalities Superficial grey matter + + + Deep grey matter - - - White matter - + - Histopathology ND ND INI Pt 7 Pt 8 CSF Normal Normal Measles antibodies Serum IgG ND Pos CSF IgG Neg Pos Measles PCR Urine ND Pos CSF Neg Neg Brain biopsy Neg * ND EEG Slowing Normal CT brain Normal Abnormal Location of MRI signal abnormalities Superficial grey matter ND + Deep grey matter - White matter - Histopathology INI ND * Post-mortem brain biopsy. ([dagger]) PCR failed on formalin fixed tissue. Pos = positive; Neg = negative; ND = not done; PLEDS = periodic lateralised epileptiform discharges; INI = intranuclear and cytoplasmic inclusion bodies.
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|Title Annotation:||ISSUES IN PUBLIC HEALTH|
|Author:||Albertyn, Christine; van der Plas, Helen; Hardie, Diana; Candy, Sally; Tomoka, Tamiwe; LeePan, Edwar|
|Publication:||South African Medical Journal|
|Date:||May 1, 2011|
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