Effectiveness of intranasal immunization with Myxovirus influenzae neuraminidase in mice]

An intranasal immunization with a A/PR8/34-isolated NA, protected mice as well as the whole virus and A/Hong Kong/1/68 virus against a subsequent infection with mice-adaptated A/PR8/34 strain.     

Mechanism of elastolysis by pancreatic elastase

Résumé Nous présentons une étude du mécanisme de l'élastolyse par une élastase partiellement purifiée du pancréas. La méthode utilisée consiste dans le dosage spectrophotométrique de l'«azoelastine» dissoute. Cette protéine n'est que très lentement hydrolysée par la trypsine et chymotrypsine cristallisées. L'élastase possède une activité protéasique considérable. L'enzyme est très rapidement adsorbée sur l'élastine. Après une incubation à pH 4,5 avec l'enzyme adsorbée, le temps de latence de l'élastolyse disparaît et la rapidité de la réaction devient proportionnelle à la concentration en élastase.     

Dosage de la procaïnestérase sérique par spectrophotométrie différentielle

Summary A method is proposed for dosage of serum procainesterase by differential spectrophotometry, based on the decrease of the optical density at 295 mµ in the course of the hydrolysis.     

Negative epistasis between the malaria-protective effects of alpha+-thalassemia and the sickle cell trait

The hemoglobinopathies, disorders of hemoglobin structure and production, protect against death from malaria. In sub-Saharan Africa, two such conditions occur at particularly high frequencies: presence of the structural variant hemoglobin S and alpha(+)-thalassemia, a condition characterized by reduced production of the normal alpha-globin component of hemoglobin. Individually, each is protective against severe Plasmodium falciparum malaria, but little is known about their malaria-protective effects when inherited in combination. We investigated this question by studying a population on the coast of Kenya and found that the protection afforded by each condition inherited alone was lost when the two conditions were inherited together, to such a degree that the incidence of both uncomplicated and severe P. falciparum malaria was close to baseline in children heterozygous with respect to the mutation underlying the hemoglobin S variant and homozygous with respect to the mutation underlying alpha(+)-thalassemia. Negative epistasis could explain the failure of alpha(+)-thalassemia to reach fixation in any population in sub-Saharan Africa.