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add missing text in templates
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fred-atherden committed Jan 15, 2025
1 parent 6f0a5a8 commit 18aeff0
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Showing 2 changed files with 5 additions and 5 deletions.
8 changes: 4 additions & 4 deletions src/related-object-workaround.xsl
Original file line number Diff line number Diff line change
Expand Up @@ -20,14 +20,14 @@
<xsl:when test="parent::p/parent::sec and ancestor::abstract">
<xsl:element name="ext-link">
<xsl:attribute name="ext-link-type">uri</xsl:attribute>
<xsl:apply-templates select="@xlink:href|*|comment()|processing-instruction()"/>
<xsl:apply-templates select="@xlink:href|*|text()|comment()|processing-instruction()"/>
</xsl:element>
</xsl:when>
<!-- This is simply included in the narrative flow: replace with a link -->
<xsl:when test="parent::p or parent::th or parent::td">
<xsl:element name="ext-link">
<xsl:attribute name="ext-link-type">uri</xsl:attribute>
<xsl:apply-templates select="@xlink:href|*|comment()|processing-instruction()"/>
<xsl:apply-templates select="@xlink:href|*|text()|comment()|processing-instruction()"/>
</xsl:element>
</xsl:when>
<!-- else: do nothing, retain it as related-object -->
Expand All @@ -53,14 +53,14 @@
<xsl:when test="position() = 1">
<xsl:element name="ext-link">
<xsl:attribute name="ext-link-type">uri</xsl:attribute>
<xsl:apply-templates select="@xlink:href|*|comment()|processing-instruction()"/>
<xsl:apply-templates select="@xlink:href|*|text()|comment()|processing-instruction()"/>
</xsl:element>
</xsl:when>
<xsl:otherwise>
<xsl:text>; </xsl:text>
<xsl:element name="ext-link">
<xsl:attribute name="ext-link-type">uri</xsl:attribute>
<xsl:apply-templates select="@xlink:href|*|comment()|processing-instruction()"/>
<xsl:apply-templates select="@xlink:href|*|text()|comment()|processing-instruction()"/>
</xsl:element>
</xsl:otherwise>
</xsl:choose>
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2 changes: 1 addition & 1 deletion test/all/kitchen-sink.xml
Original file line number Diff line number Diff line change
Expand Up @@ -88,7 +88,7 @@
<p>T cell receptors (TCRs) are formed by stochastic gene rearrangements, theoretically generating &#x003E;10<sup>19</sup> sequences. They are selected during thymopoiesis, which releases a repertoire of about 10<sup>8</sup> unique TCRs per individual. How evolution shaped a process that produces TCRs that can effectively handle a countless and evolving set of infectious agents is a central question of immunology. The paradigm is that a diverse enough repertoire of TCRs should always provide a proper, though rare, specificity for any given need. Expansion of such rare T cells would provide enough fighters for an effective immune response and enough antigen-experienced cells for memory. We show here that human thymopoiesis releases a large population of CD8<sup>&#x002B;</sup> T cells harboring &#x03B1;/&#x03B2; paired TCRs that (i) have high generation probabilities and (ii) a preferential usage of some V and J genes, (iii) are shared between individuals and (iv) can each recognize and be activated by multiple unrelated viral peptides, notably from EBV, CMV and influenza. These polyspecific T cells may represent a first line of defense that is mobilized in response to infections before a more specific response subsequently ensures viral elimination. Our results support an evolutionary selection of polyspecific &#x03B1;/&#x03B2; TCRs for broad antiviral responses and heterologous immunity.</p>
<sec>
<title>Clinical trial number:</title>
<p><ext-link ext-link-type="uri" xlink:href="https://drks.de/search/en/trial/dummy-trial"/>.</p>
<p><ext-link ext-link-type="uri" xlink:href="https://drks.de/search/en/trial/dummy-trial">dummy-trial</ext-link>.</p>
</sec>
<sec>
<title>Graphical abstract</title><fig id="figa1" position="float" orientation="portrait" fig-type="figure">
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