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1.
Clin Neurol Neurosurg ; 114(7): 852-61, 2012 Sep.
Article in English | MEDLINE | ID: mdl-22326129

ABSTRACT

BACKGROUND: Highly active antiretroviral therapy (HAART) restores the inflammatory immune response in AIDS patients and it may unmask previous subclinical infections or paradoxically exacerbate symptoms of opportunistic infections. Up to 25% of patients receiving HAART develop immune reconstitution inflammatory syndrome (IRIS). We describe six patients with IRIS central nervous system (CNSIRIS) manifestations emphasizing the relevance of CSF cultures and neuroimaging in early diagnosis and management. METHODS: Patients with CNSIRIS were identified among hospitalized HIV-infected patients that started HAART from January 2002 through December 2007 at a referral neurological center in Mexico. RESULTS: One-hundred and forty-two HIV-infected patients with neurological signs were hospitalized, 64 of which had received HAART, and six (9.3%) developed CNSIRIS. Five patients were male. Two cases of tuberculosis, two of cryptococcosis, one of brain toxoplasmosis, and one possible PML case were found. IRIS onset occurred within 12 weeks of HAART in five patients. Anti-infective therapy was continued. In one case, HAART was temporarily suspended. In long-term follow-up the clinical condition improved in all patients. CONCLUSIONS: CNSIRIS associated to opportunistic infections appeared in 9% of patients receiving HAART. Interestingly, no cases of malignancy or neoplasm IRIS-related were found. Frequent clinical assessment and neuroimaging studies supported diagnosis and treatment. Risk factors were similar to those found in other series.


Subject(s)
Acquired Immunodeficiency Syndrome/therapy , Antiretroviral Therapy, Highly Active/adverse effects , Central Nervous System Diseases/therapy , Immune Reconstitution Inflammatory Syndrome/therapy , AIDS-Related Opportunistic Infections/epidemiology , AIDS-Related Opportunistic Infections/therapy , Acquired Immunodeficiency Syndrome/complications , Adult , Anti-Bacterial Agents/therapeutic use , Antifungal Agents/therapeutic use , CD4 Lymphocyte Count , Central Nervous System Diseases/etiology , Cryptococcosis/cerebrospinal fluid , Cryptococcosis/etiology , Cryptococcosis/microbiology , Cryptococcus neoformans , Female , Humans , Immune Reconstitution Inflammatory Syndrome/etiology , Leukoencephalopathy, Progressive Multifocal/cerebrospinal fluid , Leukoencephalopathy, Progressive Multifocal/etiology , Magnetic Resonance Imaging , Male , Mexico , Mycobacterium tuberculosis , Neuroimaging , Retrospective Studies , Toxoplasmosis/cerebrospinal fluid , Toxoplasmosis/etiology , Treatment Outcome , Tuberculosis/cerebrospinal fluid , Tuberculosis/etiology , Tuberculosis/microbiology
2.
J Clin Virol ; 48(1): 6-10, 2010 May.
Article in English | MEDLINE | ID: mdl-20335066

ABSTRACT

BACKGROUND: JC virus (JCV), the causative agent of progressive multifocal leukoencephalopathy (PML), is classified in 8 different genotypes. Previous reports have suggested a positive association between specific genotypes and PML. OBJECTIVE: To compare genotypes and adaptive mutations of JCV strains from Brazilian AIDS patients with and without PML. STUDY DESIGN: The VP1 region of JCV was amplified by polymerase chain reaction from cerebrospinal fluid samples from 51 patients with PML and from urine samples of 47 patients with AIDS without central nervous system disease. Genotyping was done by phylogenetic analysis. Amino acid replacement and selection pressures were also investigated. RESULTS: JCV genotype frequency distributions showed that genotypes 2 (32.7%), 1 (26.5%) and 3 (23.5%) were the most prevalent. Genotype 1 had a positive association (p<0.0001) and genotype 3 showed an inverse association (p<0.001) with PML. A previously undescribed point mutation at residue 91 (L/I or L/V) and (L/P), non-genotype-associated, was found in 5/49 (10.2%) and 2/47 (4.3%) JCV sequences from PML and non-PML patients, respectively. This mutation was under positive selection only in PML patients. A previously described substitution of T-A in position 128 showed a significant difference between PML and non-PML cases (70% versus 16%, respectively, p<0.0005). CONCLUSION: In Brazilian patients with AIDS, JCV genotype 1 showed a strong association with PML (p<0.0001) and JCV genotype 3 showed an inverse association with PML. The possible association of aminoacids substitution in residues 91 and 128 with PML in patients with AIDS must be further investigated.


Subject(s)
HIV Infections/virology , JC Virus/genetics , Leukoencephalopathy, Progressive Multifocal/virology , Amino Acid Substitution , Bayes Theorem , Brazil , Capsid Proteins/genetics , Chi-Square Distribution , DNA, Viral/analysis , Genotype , HIV Infections/complications , Humans , Leukoencephalopathy, Progressive Multifocal/cerebrospinal fluid , Leukoencephalopathy, Progressive Multifocal/complications , Leukoencephalopathy, Progressive Multifocal/urine , Monte Carlo Method , Phylogeny , Sequence Analysis, DNA
3.
Arq Neuropsiquiatr ; 62(2B): 550-4, 2004 Jun.
Article in Portuguese | MEDLINE | ID: mdl-15273863

ABSTRACT

A case of progressive multifocal leukoencephalopathy (PML) is presented, with literature review. PML diagnosis and its differential diagnosis are presented, with emphasis on neuroradiology, cerebrospinal fluid analysis and polymerase chain reaction studies. The prognosis of PML is usually poor, with a median survival of 1-6 months. There is yet no proven effective treatment for this condition; HAART has become the standard of care for these patients.


Subject(s)
AIDS-Related Opportunistic Infections/diagnosis , JC Virus/isolation & purification , Leukoencephalopathy, Progressive Multifocal/diagnosis , Polymerase Chain Reaction , AIDS-Related Opportunistic Infections/cerebrospinal fluid , AIDS-Related Opportunistic Infections/virology , Diagnosis, Differential , Fatal Outcome , Female , Humans , Leukoencephalopathy, Progressive Multifocal/cerebrospinal fluid , Leukoencephalopathy, Progressive Multifocal/virology , Magnetic Resonance Imaging , Middle Aged
4.
Arq. neuropsiquiatr ; Arq. neuropsiquiatr;62(2b): 550-554, jun. 2004. ilus
Article in Portuguese | LILACS | ID: lil-362228

ABSTRACT

Relatamos um caso de leucoencefalopatia multifocal progressiva, doença infecciosa desmielinizante do sistema nervoso central, seguido de revisão da literatura. Comenta-se a importância diagnóstica dos métodos de imagem, bem como da análise do líquor e da técnica de reação em cadeia da polimerase (PCR). Até o presente momento, não há terapia efetiva para a condição, com sobrevida média de 1-6 meses nos pacientes não tratados; evolução favorável pode ocorrer no subgrupo de pacientes que obtém melhora da imunidade com o uso de terapia anti-retroviral.


Subject(s)
Humans , Female , Middle Aged , AIDS-Related Opportunistic Infections/diagnosis , JC Virus/isolation & purification , Leukoencephalopathy, Progressive Multifocal/diagnosis , Polymerase Chain Reaction , AIDS-Related Opportunistic Infections/cerebrospinal fluid , AIDS-Related Opportunistic Infections/virology , Diagnosis, Differential , Fatal Outcome , Leukoencephalopathy, Progressive Multifocal/cerebrospinal fluid , Leukoencephalopathy, Progressive Multifocal/virology , Magnetic Resonance Imaging
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