Efficient reconstruction of dielectric objects based on integral equation approach with Gauss-Newton minimization.

Reconstruction of unknown objects by microwave illumination requires efficient inversion for measured electromagnetic scattering data. In the integral equation approach for reconstructing dielectric objects based on the Born iterative method or its variations, the volume integral equations are involved because the imaging domain is fully inhomogeneous. When solving the forward scattering integral equation, the Nyström method is used because the traditional method of moments may be inconvenient due to the inhomogeneity of the imaging domain. The benefits of the Nyström method include the simple implementation without using any basis and testing functions and low requirement on geometrical discretization. When solving the inverse scattering integral equation, the Gauss-Newton minimization approach with a line search method (LSM) and multiplicative regularization method (MRM) is employed. The LSM can optimize the search of step size in each iteration, whereas the MRM may reduce the number of numerical experiments for choosing the regularization parameter. Numerical examples for reconstructing typical dielectric objects under limited observation angles are presented to illustrate the inversion approach.

An attenuated EIAV vaccine strain induces significantly different immune responses from its pathogenic parental strain although with similar in vivo replication pattern.

The EIAV (equine infectious anemia virus) multi-species attenuated vaccine EIAV(DLV121) successfully prevented the spread of equine infectious anemia (EIA) in China in the 1970s and provided an excellent model for the study of protective immunity to lentiviruses. In this study, we compared immune responses induced by EIAV(DLV121) to immunity elicited by the virulent EIAV(LN40) strain and correlated immune responses to protection from infection. Horses were randomly grouped and inoculated with either EIAV(DLV121) (Vaccinees, Vac) or a sublethal dose of EIAV(LN40) (asymptomatic carriers, Car). Car horses became EIAV(LN40) carriers without disease symptoms. Two of the four Vac horses were protected against infection and the other two had delayed onset or reduced severity of EIA with a lethal EIAV(LN40) challenge 5.5 months post initial inoculation. In contrast, all three Car animals developed acute EIA and two succumbed to death. Specific humoral and cellular immune responses in both Vac and Car groups were evaluated for potential correlations with protection. These analyses revealed that although plasma viral loads remained between 10(3) and 10(5)copies/ml for both groups before EIAV(LN40) challenge, Vac-treated animals developed significantly higher levels of conformational dependent, Env-specific antibody, neutralizing antibody as well as significantly elevated CD4(+) T cell proliferation and IFN-γ-secreting CD8(+) T cells than those observed in EIAV(LN40) asymptomatic carriers. Further analysis of protected and unprotected cases in vaccinated horses identified that cellular response parameters and the reciprocal anti-p26-specific antibody titers closely correlated with protection against infection with the pathogenic EIAV(LN40). These data provide a better understanding of protective immunity to lentiviruses.

[The difference in specific humoral immune responses induced with the attenuated equine infectious anemia vaccine strain and virulent strain.].

AIM: To disclose the potential roles of humoral immune response in the EIAV vaccine-induced protective immunity. In this study, major parameters of humoral immunity be compared between horses inoculated with the EIAV vaccine strain and the pathogenic virulent strain. METHODS: Experimental horses were randomly assigned into the group inoculated with the vaccine strain EIAV(DLV); (the vaccinated group) and the group inoculated with sub-morbigenous dose of virulent strain EIAV(Liao); (the inapparent infection group). Humoral immunity parameters, including binding endpoint titer and avidity index of antibodies to the envelop protein (Env) and the capsid protein (P26), and the conformation-dependent index of the Env antibody, were assayed and compared between these two groups by using ELISA. Neutralizing antibodies to the EIAV vaccine strain and a pathogenic strain were simultaneously detected by using plaque forming unite assay (PFU) and reverse transcriptase activity assay, respectively. RESULTS: In general, all humoral parameters increased with a time-dependent manner in both the vaccinated and the inapparent infection group. However, significantly higher antibody activities for P26 binding endpoint titer and Env avidity index were detected in the vaccinated group within 2 months post infection (P<0.05). Furthermore, the conformation-dependent index of the Env antibody in the vaccinated group was significantly higher than that in the inapparent infection group throughout the entire observation period (P<0.05). The most dramatic difference between these experimental groups was in the raise of the neutralizing antibody. The antibody neutralizing both the vaccine strain EIAV(DLV); and a virulent strain EIAV(DLV34); was detected significantly earlier and in higher titers in vaccinated horses than in virulent strain-infected horses (P<0.01 for EIAV(FDDV); and P<0.05 for EIAV(DLV34);). CONCLUSION: Statistically significant differences in EIAV-specific binding antibodies and the neutralizing antibody are detected between animals induced with the EIAV vaccine strain and the virulent strain. Importantly, the significantly early and strong responses in the neutralizing antibody and the conformation-dependent Env antibody induced by the vaccine implicate special roles these antibodies playing in EIAV vaccine-induced immune protection.