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Although full-length viral DNA integration has been reported with another Herpesviridae family member, EBV, host chromosomal integration by HHV-6 is most consistently observed [1, 11].
The pattern of transient, primarily mild to moderate systemic adverse events has been reported with another AMA-1 antigen adjuvanted with AS02 [41].
Similar adverse effects have been reported with another γ-secretase inhibitor, avagacestat [ 6].
Failure to correctly identify B. pseudomallei has also been reported with another widely used automated system, the Vitek2 system (7 ).
However, severe pulmonary adverse events, including fatalities had been reported with another EGFR-inhibitor (gefinitib-Iressa®)[ 3].
No data of CD8+ T cell immune-suppression have been reported with another derived-microbial epitopes in humans infected with T. cruzi.
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However, the result should be interpreted with caution because a similar pattern was observed in the values of KM for the substrate used in the assays (see Materials and Methods) and comparable values were reported with another substrate [40], [41].
Recently, promising results have been reported with the addition of another monoclonal antibody, lumiliximab, to the FCR schedule.
Similar experiences have also been reported with Shigella dysenteriae type 1, another enteric pathogen that causes life-threatening disease and has epidemic potential.
Similar results have also been reported with the irinotecan-gemcitabine regimen by another research group (Rocha-Lima et al, 2002).
Similar results were reported with exemestane, another AI, confirming its superiority over tamoxifen in the neoadjuvant setting (Semiglazov et al, 2005), but a small randomised trial has suggested that it may be inferior to letrozole (Chow et al, 2008).
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