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Human cysticercosis: parasitology, pathology, clinical manifestations and available treatment.

Human cysticercosis is a global health problem and neurocysticercosis a serious clinical syndrome. The diagnosis of neurocysticercosis can now be made with a high degree of accuracy by scrutiny of clinical signs and symptoms in combination with X-ray, computed tomography or magnetic resonance imaging, serological tests and laboratory examinations. Differential clinical diagnosis with tumor, and vascular and inflammatory conditions, may however, prove difficult in nonendemic areas. The management of cysticercosis has been radically changed by the advent of effective chemotherapy. Both the heterocyclic pyrazinoisoquinoline compound, praziquantel and the benzimidazole carbamate, albendazole, have now been extensively tested and successfully used for treatments of neurocysticercosis, usually in combination with corticosteroids. The definition of appropriate criteria and guidelines for the use of chemotherapy, may however, require further research. Surgical interventions continue to play an important role in certain clinical presentations. Recent advances in immunological research hold realistic promise for the development of a vaccine against Taenia solium.

Animals↗

The parasitology of malaria and the study of protective immunity.

Phenotypic antigenic variation within parasite strains and antigenic diversity between strains are important parameters in understanding the development of immunity to malaria. With the Plasmodium chabaudi chabaudi model in inbred mice, a combination of serological tests and DNA technology can be used to study the specificity of inducer and effector mechanisms in an infection with characteristics similar in many ways to those of P. falciparum in man.

Animals↗

Measuring cellular immune responses to malaria antigens in endemic populations: epidemiological, parasitological and physiological factors which influence in vitro assays.

Measurements of in vitro cellular immune responses to malaria antigens are influenced by a variety of external factors. The physiological status of the donor, which is affected by, for example, malaria infection, intercurrent illness and pregnancy, can influence the lymphoproliferative response to specific antigens. Prior exposure to malaria antigens, determined by malaria endemicity, seasonal variations in transmission and the degree of polymorphism of the particular antigen, will also affect the prevalence and intensity of responses. Malaria-related immunosuppression may be both generalised and antigen specific. Although in vitro responses to malaria antigens are profoundly suppressed in acutely infected individuals, there is evidence that lymphocyte activation does occur in vivo. We conclude that longitudinal studies, correlating specific immune responses with subsequent malaria morbidity are required, to identify potentially protective antigens and appropriate effector mechanisms.

Acute Disease↗

Choice of sample size in parasitological experiments.

One of the most awkward practical problems confronting a research worker setting up an experiment is to decide how big the experiment should be. The larger the number of subjects then the smaller is the degree of uncertainty in the conclusions; but large trials are costly and may have to be of long duration, so there is every incentive to keep trials as small as possible. Statistics is the science of coping; with uncertainty, and in this article Michael Healy explains the statistical basis that helps to decide how big a sample size should be - how to balance minimum error rates with optimal cost efficiency.

Journal Article↗

Parasitology Today readership survey.

Our February readership survey gave interesting information, and some fairly universal cris de coeur - especially about the lack of funds available to support field research. You were critical of the journal's delivery times - which, for various reasons, should now improve - but in amongst the compliments and undisguised flattery were some real gems. I want to thank all of you who sent in completed replies, and here I have attempted to summarize some of the most significant trends suggested by your responses.

Journal Article↗

Mosquito salivary glands: Parasitological and molecular aspects.

The salivary glands of mosquitoes serve in sugar feeding and blood vessel location. Components have been recently identified that may function in sugar feeding and digestion and platelet anti-aggregation. These factors correlate with salivary gland structure and appear to be controlled differentially in female mosquitoes. Analysis of gene expression has led to the discovery of three novel moieties in saliva: two involved in sugar feeding and one, specific to female mosquitoes, which is probably involved in blood feeding. Studies of parasite involvement in the salivary glands and host haemostasts have shown that parasites target specific interactions and modify them to enhance transmission. Here, Anthony James and Philippe Rossignol present an overview of mosquito salivary gland morphology and function, discuss recent advances in salivary gland molecular biology that have led to the discovery of new components and describe how parasites may modify salivary function to enhance transmission,.

Journal Article↗

Application of 3-d computer-aided reconstruction in parasitology.

Three-dimensional (3-D) reconstruction is sometimes useful to describe the fine morphology of the subcellular organization of parasites. Francois Polluoult, Bruno Pietrzyk, Eduardo Dei-Cas and Daniel Camus show how computer-aided reconstruction from serial sections is done.

Journal Article↗